Hammons, P. v. Ethicon, Inc.

J-A25032-17

2018 PA Super 172

PATRICIA L. HAMMONS IN THE SUPERIOR COURT
OF
PENNSYLVANIA

v.

ETHICON, INC., JOHNSON & JOHNSON;
GYNECARE; SECANT MEDICAL; SECANT
MEDICAL, INC.; PRODESCO, INC.; AND
SECANT MEDICAL, LLC

Appeal of Patricia L. Hammons No. 1522 EDA 2016

Appeal from the Judgment Entered April 14, 2016
In the Court of Common Pleas of Philadelphia County
Civil Division at No: 3913 MAY TERM 2013

PATRICIA L. HAMMONS IN THE SUPERIOR COURT
OF
PENNSYLVANIA

v.

ETHICON, INC., JOHNSON & JOHNSON;
GYNECARE; SECANT MEDICAL; SECANT
MEDICAL, INC.; PRODESCO, INC.; AND
SECANT MEDICAL, LLC

APPEAL OF ETHICON, INC., JOHNSON &
JOHNSON; GYNECARE; SECANT
MEDICAL; SECANT MEDICAL, INC.;
PRODESCO, INC.; AND SECANT
MEDICAL, LLC

No. 1526 EDA 2016

Appeal from the Judgment Entered April 14, 2016
In the Court of Common Pleas of Philadelphia County
Civil Division at No: 3913 MAY TERM 2013
J-A25032-17

BEFORE: OTT, STABILE, JJ. and STEVENS,* P.J.E.

OPINION BY STABILE, J.: FILED JUNE 19, 2018

In this product liability action, Appellants, Ethicon, Inc. and Johnson &

Johnson, Ethicon’s parent company (collectively “Ethicon”) and Appellee,

Patricia Hammons (“Hammons”), appeal and cross-appeal, respectively, from

a judgment of $12,850,945.18 entered in favor of Hammons in the

Philadelphia Court of Common Pleas. Hammons alleged that she suffered

injuries caused by Ethicon’s negligent design of, and failure to provide

adequate warnings about, the Prolift Kit, a medical product used to treat

prolapsed pelvic organs. Appellants challenge the trial court’s denial of (1)

their preliminary objections alleging lack of specific personal jurisdiction, (2)

their post-trial motions seeking judgment n.o.v. on the basis of the statute of

limitations and Appellee’s failure to present sufficient evidence, (3) their post-

trial motions seeking a new trial based on the trial court’s evidentiary and

instructional errors, (4) their post-trial motions seeking remittitur on the

compensatory damage verdict and vacatur or remittitur of the punitive

damage verdict. In her cross-appeal, Hammons argues that the trial court

erred by awarding delay damages only on the compensatory damage verdict

instead of the entire verdict. We affirm in all respects.

____________________________________________

* Former Justice specially assigned to the Superior Court.

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FACTUAL AND PROCEDURAL HISTORY

Johnson & Johnson has its worldwide headquarters in New Jersey.

Ethicon is a wholly owned subsidiary of Johnson & Johnson with a principal

place of business in New Jersey. As discussed in greater detail below, Ethicon

worked closely with other entities and individuals in Pennsylvania to design,

test and manufacture the Prolift Kit (“Prolift”).

Our review of the record reveals the following. Pelvic organ prolapse is

a pelvic floor disorder that affects the muscles and tissues that hold the pelvic

organs, including the bladder, uterus, vagina, small bowel, and rectum, in

place. Due to childbirth, advancing age, or other causes, these muscles and

tissues can weaken, and one or more pelvic organs “prolapse,” or descend

into or outside of the vaginal canal or anus. Pelvic organ prolapse is

accompanied by a number of other symptoms, including a bulge or feeling of

fullness in the pelvic area, back problems, pain during sexual intercourse,

urinary problems such as leaking of urine or a chronic urge to urinate, or

constipation.

In the early 2000s, a group of surgeons in France developed Prolift in

an attempt to improve treatment of pelvic repairs. In 2005, Ethicon brought

Prolift to market. Prolift includes a precut piece of surgical mesh and single–

use implanting tools called trocars. The mesh is woven from non-absorbable

polypropylene sutures and is pre-cut into distinct shapes for anterior, posterior

or total pelvic repairs. During implantation, the mesh is inserted into the

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patient’s body through the vagina, pulled through the vaginal wall, placed to

support prolapsed pelvic organs and anchored with mesh “arms” through a

woman’s bones and muscles via trocars. Prolift surgery is a quality-of-life

decision.

In 2009, Hammons, a post-menopausal woman who lives with her

boyfriend in Washington, Indiana, was diagnosed with prolapse of her uterus

and bladder. Her physician, Michael Baker, D.O., recommended surgical

repair of her bladder prolapse and removal of her uterus and ovaries. On May

5, 2009, Hammons signed a consent form authorizing a total vaginal

hysterectomy and “anterior repair with mesh.” Defense Trial Exhibit (“DTX”)-

36. The form stated that Dr. Baker advised Hammons why the procedure was

necessary, “the risks thereof, [and] its advantages and possible complications

. . . .” Id. On the same date, Dr. Baker performed the surgery and implanted

the Prolift device in Hammons’ body to support her organs. Dr. Baker wrote

in his report of the operation, “I discussed the . . . risk of injury to bowel,

bladder or ureter as well as . . . having pain with intercourse or other types of

pain following surgery. [Hammons] agreed to these risks and wishes to

proceed with surgery despite these risks.” DTX-37 at 208-09. Hammons

testified, however, that Dr. Baker did not tell her prior to surgery that pain

during sexual intercourse was one of the risks of surgery. Notes of Testimony

(“N.T.”), 12/11/15 (PM), at 32.

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On July 20, 2009, Hammons returned to Dr. Baker with complaints of

pinching and sharp pain that caused her to stop engaging in intimate relations.

Dr. Baker noted sexual dysfunction but did not offer a causal explanation.

During the next visit, Dr. Baker diagnosed Hammons with rectal prolapse, or

rectocele. She sought referral to a different gynecologist, Dr. Lackey.

In November 2009, Dr. Lackey diagnosed Hammons with pelvic

pressure and incontinence, rectocele, a tear in the vaginal septum and

dyspareunia (pain during sexual intercourse). In December 2009, Dr. Lackey

surgically repaired the rectocele by using Hammons’ own tissue to provide

support for her rectum. In January 2010, Dr. Lackey told Hammons that she

could resume sexual intercourse. It appears that Hammons did not visit Dr.

Lackey again until January 2012.

On August 16, 2011, Hammons signed a form authorizing the release of

her “implant related medical records” for use in “plaintiff litigation for product

liability.” DTX-42; N.T., 12/11/15 (PM), at 63.

In January 2012, Hammons returned to Dr. Lackey complaining of pain

during intercourse. Dr. Lackey did not identify Prolift as the cause of

Hammons’ discomfort. On August 14, 2012, Hammons returned to Dr. Lackey

complaining of incontinence and recurrent prolapse. Dr. Lackey referred

Hammons to urogynecologist Michael Heit in Louisville, Kentucky.

On August 30, 2012, Dr. Heit diagnosed Hammons with symptoms

caused by implantation of Prolift mesh and recommended additional surgeries

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for excision of the mesh and repair of the entire pelvic floor. In November

2012, Dr. Heit surgically excised mesh from Hammons’ anterior vaginal wall,

repaired two cystotomies (holes in her bladder), placed a ureteral stent and

repaired her recurring rectocele. In January 2013, Dr. Heit removed the

ureteral stent, noting new penetration of mesh into the left lateral bladder

wall. Dr. Heit surgically removed additional mesh from her bladder. In all,

Dr. Heit performed three surgeries.

Hammons continues to suffer from incontinence and pain during

intercourse. Because of pain, and because her vagina is shortened and rigid

with scar tissue, she has abstained from sex, causing humiliation and

impairing her relationship with her boyfriend.

On May 31, 2013, Hammons filed a civil complaint against Ethicon in

the Philadelphia Court of Common Pleas (“trial court”) alleging negligence,

strict liability and other torts at May Term, 2013, No. 3913 (“Individual

Docket”). In March 2014, the trial court transferred Hammons’ case to a Mass

Tort Program action, In Re Pelvic Mesh Litigation, which encompassed all

pelvic mesh cases pending in Philadelphia.

On March 31, 2014, the trial court issued a case management order

dividing the Pelvic Mesh Litigation matter into proceedings on a Master Docket

and proceedings on each plaintiff’s Individual Docket.1 On the Master Docket,

____________________________________________

1The order referred to each plaintiff’s individual docket as the “Original
Docket.” We substitute the term “Individual Docket” for “Original Docket.”

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all pelvic mesh plaintiffs collectively were to file a “long form” complaint

alleging facts and causes of action that applied globally to all pelvic mesh

cases, and each defendant was to file (1) preliminary objections that raised

global objections to all pelvic mesh cases or (2) an answer to the long form

complaint. Within 25 days after the answer to the long form complaint, each

plaintiff was to file a “short form” complaint on her Individual Docket

identifying the counts of the long form complaint that she incorporated by

reference and asserting any new facts or causes of action not in the long form

complaint. Each defendant could then file preliminary objections on the

Individual Docket raising objections that applied specifically to the short form

complaint. If the defendant did not file preliminary objections, an entry of

appearance by counsel for the defendant would constitute a denial of

allegations in the short form complaint and an assertion of all applicable new

matter and defenses.

On May 14, 2014, the plaintiffs filed an eighteen-count long form

complaint on the Master Docket against Ethicon and other defendants,

including Secant Medical, Inc. and Secant Medical LLC (“Secant”), a

manufacturer of surgical mesh located in Perkasie, Pennsylvania. Among the

counts in the long form complaint were strict liability actions for design defect,

manufacturing defect and failure to warn. The long form complaint also

asserted that personal jurisdiction existed over Ethicon in Pennsylvania.

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J-A25032-17

On May 21, 2014, the plaintiffs served Ethicon with the long form

complaint. On June 10, 2014, Ethicon filed preliminary objections to the long

form complaint arguing that eleven of the eighteen counts failed to state a

cause of action and objecting to the lack of specificity of certain averments.

Ethicon did not file any objection to personal jurisdiction. Secant also filed

preliminary objections seeking dismissal of the claims under the Biomedical

Access Assurance Act, 21 U.S.C. § 1601 et seq. On August 22, 2014, the trial

court sustained Secant’s preliminary objections and dismissed all claims

against Secant with prejudice. On September 2, 2014, the trial court

overruled Ethicon’s preliminary objections. On September 23, 2014, Ethicon

filed an answer to the long form complaint with new matter.

On October 7, 2014, Hammons filed a short form complaint on her

Individual Docket. On October 28, 2014, Ethicon filed preliminary objections

to the short form complaint asserting lack of personal jurisdiction. On

November 6, 2014, the trial court entered an order on the Master Docket

directing the parties to take discovery on the jurisdictional issue. On March

30, 2015, the trial court overruled Ethicon’s motion on the Master Docket to

dismiss for lack of personal jurisdiction and Ethicon’s preliminary objections

on Hammons’ Individual Docket asserting lack of personal jurisdiction. The

trial court did not provide any explanation for its ruling.

On August 31, 2015, Ethicon moved for summary judgment on the

Individual Docket. Among other arguments, Ethicon claimed that it was

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entitled to summary judgment on Hammons’ manufacturing defect claim

because there was no evidence that the Prolift device used in her surgery

deviated from its intended design. On November 24, 2015, the trial court

granted summary judgment to Ethicon on the manufacturing defect claim and

other claims. The court left intact Hammons’ design defect and failure-to-

warn claims.

Hammons’ expert witnesses, gynecologist Daniel Elliott, M.D., and

urogynecologist Anne Weber, M.D., testified that Prolift was defectively

designed. Dr. Elliott testified that Prolift’s mesh contains too much suture for

implantation through the wall of the vagina. Prolift also requires implantation

of approximately 260 yards of a plastic material foreign to the patient’s body.

Dr. Elliott testified that the mesh is over-engineered and too heavy and dense,

and the pores of the mesh are too small for the product to perform properly

and as intended. Another expert, Uwe Klinge, M.D., opined that Prolift mesh’s

one millimeter pores were inadequate. He testified Ethicon should have used

a mesh with pores larger than three millimeters. Plaintiff’s Exhibit (“P-”) 3401

at 10-15; P-3402 at 12-17; P-3408 at 4-10.

Dr. Elliott also testified that the process of implantation recommended

by Ethicon actually causes Prolift’s mesh pores to collapse. For instance, he

explained, pores collapse because the vagina is a dynamic organ that moves,

shifts, and changes shape with normal movement. Pores also collapse

because implantation requires a physician to pull on the mesh to guide it

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through the vagina, the vaginal wall, and pelvic muscles to anchor it into place.

Lastly, pores collapse when physicians cause tension in the mesh when they

pull it under the bladder. Ethicon knew the vagina and pelvic organs create

an environment different from any other (such as the abdominal cavity for

which the mesh was created) but failed to modify the Prolift mesh and surgical

techniques to account for the differences. P-3402 at 27-37; P-3407 at 1-7;

P-3408, at 10-17; P-3415 at 6-7.

Dr. Elliott testified that implantation of materials foreign to the body

naturally causes chronic foreign body reaction and inflammatory response,

and Prolift causes severe inflammatory reaction proportional to the large

amount of plastic used. Severe inflammation causes scar tissue formation.

Prolift mesh’s small pores and pore collapse impede normal tissue growth

through the pores. The mesh bands and rolls to exacerbate the inflammatory

and scar formation cycle. The process results in platting or bridging, that is,

scar tissue becomes rigid, contracts and bunches. As the mesh contracts, it

erodes layers of tissue in the vagina and then in neighboring organs. It can

become exposed in the vagina and damage the bladder, intestines and other

organs, which then might experience dysfunction. Further, mesh that

contracts causes tissue irritation and pulls painfully on the patient’s muscles,

causing chronic muscle pain and pelvic floor muscle spasms. Dr. Elliott

testified that the inflammatory response is chronic and triggers a progressive

cycle of mesh contraction and erosion that causes pain response and organ

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dysfunction. He added that pain management techniques are generally

unsuccessful, and that Prolift’s design precludes successful and complete

excision without risk of “severe damage” to the pelvic structures. P-3401 at

2-13; P-3402, at 12-37.

Dr. Elliott and Dr. Weber added that Prolift has limited effectiveness in

repairing prolapse. Dr. Elliott testified that Ethicon’s pre-launch clinical study

data indicated more than a twenty percent rate of prolapse recurrence at both

six and twelve months following Prolift implantation. Even by Ethicon’s

predefined criteria, Prolift failed performance expectations because prolapse

recurs frequently and shortly after implantation. Dr. Weber testified that she

independently analyzed raw clinical data and concluded Ethicon underreported

the true rate of recurrence by ten percent. Dr. Weber also noted the existence

of clinical experience and studies known to Ethicon that demonstrated nearly

twenty percent of women suffered mesh shrinkage with pain during

intercourse, and another approximately twenty percent suffered mesh

erosions within a year of implantation. N.T., 12/8/15 (A.M.), at 23-64; P-

3401 at 6; P-3402, at 21-24; P-3404 at 18; P-3415 at 7.

Dr. Elliott and Dr. Weber concluded that Prolift is unsafe. Dr. Elliott

further testified that Ethicon’s product warnings were inadequate, because

they failed to convey all of the risks of the product, including severe and

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permanent pain during sexual intercourse.2 Dr. Baker, the surgeon who

implanted the Prolift device, testified that he would not have recommended

the product had Ethicon adequately warned him of its risks. Moreover, Ethicon

knew about the risks of the product before placing it on the market. Prolift’s

inventors, Professor Jacquetin and Dr. Cosson, insisted both before and after

Prolift’s launch on replacement of the Prolene/Gynemesh mesh with a safer

mesh alternative called Ultrapro. Dr. Weber agreed that Ultrapro mesh

reduced the risk because it contained less mesh, had larger pores and was

softer in place. Ultrapro’s characteristics were thought to reduce inflammation

and scar plating. N.T., 12/7/15 (A.M.), at 57-95; N.T., 12/7/15 (P.M.), at

237-48; P-3401 at 2-3, 9-12; P-3402, at 5-7, 33-35; P-3404, at 9; P-3407 at

8-12; P-3415, at 7-8; P-3417 at 1-4.

The parties agreed that Indiana law defines the elements of Hammons’

product liability claims, while New Jersey law provides the standards for

determining punitive damages.3, 4 At the end of a three-week trial, the trial

court denied Ethicon’s motion for directed verdict. On December 21, 2015,

____________________________________________

2We discuss the question of whether Ethicon failed to provide adequate
warnings in greater depth below. See pp. 37-46, infra.

3 To the extent the parties agree on the governing law, we accept their
agreement for purposes of our decision, and we see no need to explore the
reasons for their agreement.

4 The parties do not agree whether Pennsylvania or Indiana law applies to
Ethicon’s post-trial motion to reduce the amount of Hammons’ compensatory
damages. We resolve this issue infra at pp. 68-69.

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the jury returned a verdict that Ethicon was liable for causing Hammons’

injuries and awarded compensatory damages of $5.5 million. After additional

evidence, argument, and instructions, on December 22, 2015, the jury

assessed an additional $7 million in punitive damages. Both sides filed post-

trial motions. The trial court denied Ethicon’s post–trial motions and granted

delay damages upon only the compensatory award rather than the entire

verdict. On May 12, 2016, Hammons filed a praecipe to enter judgment in

the amount of $12,850,945.18 on the Individual Docket. Both sides filed

timely notices of appeal and timely Pa.R.A.P. 1925(b) statements of errors

complained of on appeal.

ISSUES RAISED ON APPEAL

In its appeal at 1526 EDA 2016, Ethicon raises ten issues that we have

re-ordered for the sake of convenience:

1. Did the trial court commit legal error by exercising personal
jurisdiction over [Ethicon], even though [Ethicon is not]
incorporated in [and does not] maintain [its] principal place[] of
business in Pennsylvania, and even though [Hammons’] claims do
not arise from or relate to any of [Ethicon]’s contacts with
Pennsylvania?

2. Did the trial court commit legal error when it denied [Ethicon]’s
directed-verdict and JNOV motions, where [Hammons’] claims
were barred by the statute of limitations and [Hammons] did not
present legally sufficient evidence that Indiana’s discovery rule
extended the limitations period?

3. Did the trial court commit legal error when it denied [Ethicon]’s
directed-verdict and JNOV motions, where [Hammons] failed to
present legally sufficient evidence that an inadequacy in Prolift’s
warnings caused her alleged injuries?

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4. Did the trial court commit legal error when it denied [Ethicon]’s
directed-verdict and JNOV motions, where [Hammons] failed to
present legally sufficient evidence that a safer alternative design
to the Prolift medical device was available at the time of her May
2009 implantation?

5. Did the trial court commit reversible error by refusing to instruct
the jury that, to prevail on the design-defect claim, [Hammons]
was required to show a safer alternative design to Prolift?

6. Did the trial court commit legal error when it denied [Ethicon]’s
directed-verdict and JNOV motions, where [Hammons] failed to
present legally sufficient evidence that a defect in Prolift, as
opposed to potential alternatives, caused her alleged injuries?

7. Did the trial court commit reversible error by admitting
evidence and allowing argument that [Ethicon] supposedly
spoliated evidence, when there was no showing or finding that
spoliation occurred or that [Hammons] was prejudiced?

8. Did the trial court commit reversible error by instructing the
jury that [Ethicon]’s awareness of any potential misuse of Prolift
by surgeons made them responsible for all misuses of Prolift,
whether or not they were foreseeable?

9. Did the trial court err when it refused to remit the compensatory
damages award?

10. Did the trial court err when it denied [Ethicon]’s directed-
verdict and JNOV motions as to punitive damages?

Ethicon’s Brief at 3-5.

Hammons raises the following issue in her appeal at 1522 EDA 2016:

“Did the trial court improperly mold the jury’s verdict to add delay damages

calculated only on the compensatory portion of the verdict?” Hammons’ Brief

at 4.

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PERSONAL JURISDICTION

Ethicon first asserts that the trial court erroneously denied its

preliminary objections to Hammons’ Short Form Complaint, in which Ethicon

argued that personal jurisdiction does not exist over Ethicon in Pennsylvania.5

In support of this argument, Ethicon relies on the United States Supreme

Court’s recent decision in Bristol–Myers Squibb Co. v. Superior Court of

California, San Francisco County (“Bristol-Myers”), — U.S. —, 137 S.Ct.

1773 (2017), which held that California courts lacked specific jurisdiction to

entertain product liability claims by nonresidents against a nonresident drug

manufacturer, where the nonresidents were not prescribed the drug in

California and did not purchase, ingest or suffer injury from the drug there.

Hammons responds that Ethicon waived this issue by failing to raise it in

preliminary objections to the Long Form Complaint on the Master Docket. In

any event, Hammons continues, Bristol-Myers actually supports the

conclusion that “the trial court properly exercised specific jurisdiction over

Ethicon, given Ethicon’s activities in Pennsylvania relating to this case.”

Hammons’ Supplemental Brief at 1.

We conclude that Ethicon did not waive this issue, because the case

management order for pelvic mesh cases did not require Ethicon to contest

personal jurisdiction in preliminary objections to the Long Form Complaint.

____________________________________________

5We note that Ethicon raised this issue in its Pa.R.A.P. 1925(b) statement,
but the trial court did not analyze it in its opinion.

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To begin with, the case management order was a valid exercise of the

court’s authority. In 1992, the Philadelphia Court of Common Pleas initiated

the Mass Tort Program to deal efficiently with large numbers of complex but

similar tort cases by coordinating and streamlining pleadings, discovery,

pretrial motions, and trial. The legal foundation for the Program is Pa.R.Civ.P.

213, which authorizes courts to consolidate related cases and issue case

management orders for their efficient disposition. See Pa.R.Civ.P. 213(a) (“In

actions pending in a county which involve a common question of law or fact .

. . the court on its own motion . . . may order the actions consolidated[] and

may make orders that avoid unnecessary cost or delay”). The case

management order in this case—which appears to be a standard order in all

Philadelphia mass tort cases—fits well within the boundaries of Rule 213(a) by

delineating applicable procedures in pelvic mesh cases.

The case management order restricts preliminary objections to the Long

Form Complaint to issues that apply to all pelvic mesh cases. The question

whether the trial court had personal jurisdiction over Ethicon did not apply to

all pelvic mesh cases. While a question of personal jurisdiction over Ethicon

exists with regard to out-of-state plaintiffs such as Hammons, it appears fairly

certain personal jurisdiction would exist over Ethicon in actions brought by

plaintiffs who underwent Prolift surgery in Pennsylvania due to the “affiliation

between the forum and the underlying activity.” Bristol-Myers, 137 S.Ct. at

1781 (“In order for a court to exercise specific jurisdiction over a claim, there

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must be an affiliation between the forum and the underlying controversy,

principally, [an] activity or an occurrence that takes place in the forum State

. . . When there is no such connection, specific jurisdiction is lacking regardless

of the extent of a defendant's unconnected activities in the State”). Thus,

Ethicon was not required to raise objections to personal jurisdiction in

preliminary objections to the Long Form Complaint on the Master Docket.

Indeed, as Ethicon observes, it was impossible for Ethicon to challenge

personal jurisdiction in preliminary objections to the Long Form Complaint,

because this complaint “lacked any of the plaintiff-specific allegations required

to assert such objections—for example, the state where the plaintiff resides,

the state where she had the device implanted, and the state where the injury

occurred . . . When [Hammons] filed her short-form complaint that added

those allegations . . . [Ethicon] promptly and timely filed their preliminary

objetions to personal jurisdiction.” Ethicon’s Reply Brief, at 3.

On the merits, however, we conclude that personal jurisdiction exists

over Ethicon in this case. The trial court applies the following standards to

preliminary objections asserting lack of personal jurisdiction:

When preliminary objections, if sustained, would result in the
dismissal of an action, such objections should be sustained only in
cases which are clear and free from doubt. Moreover, when
deciding a motion to dismiss for lack of personal jurisdiction the
court must consider the evidence in the light most favorable to
the non-moving party. A defendant making a challenge to the
court’s personal jurisdiction has, as the moving party, the burden
of supporting its objection to jurisdiction.

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De Lage Landen Services, Inc. v. Urban Partnership, LLC, 906 A.2d 586,

589 (Pa. Super. 2006) (citation omitted). “Our standard of review of an order

of the trial court overruling . . . preliminary objections is to determine whether

the trial court committed an error of law. [Furthermore], the appellate court

must apply the same standard as the trial court.” Id.

The Due Process Clause of the Fourteenth Amendment to the United

States Constitution limits the authority of a state to exercise in personam

jurisdiction over non-resident defendants. Burger King Corp. v.

Rudzewicz, 471 U.S. 462, 471–72 (1985). The extent to which the Due

Process Clause proscribes jurisdiction depends on the nature and quality of

the defendant’s contacts with the forum state. Id. at 474–76; Kubik v.

Letteri, 614 A.2d 1110, 1114 (Pa. 1992). Where a defendant “has

established no meaningful contacts, ties or relations” with the forum, the Due

Process Clause prohibits the exercise of personal jurisdiction. Burger King,

471 U.S. at 472. However, where a defendant has “purposefully directed” his

activities at the residents of the forum, he is presumed to have “fair warning”

that he may be called to suit there. Id.

Since International Shoe Co. v. Washington, 326 U.S. 310, 317-18

(1945), the Supreme Court has recognized two types of personal jurisdiction:

general and specific. Id., 326 U.S. at 317-18. The court has general

jurisdiction over a foreign corporation when its affiliations with the state are

so “continuous and systematic” as to render them essentially at home in the

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forum State. Goodyear Dunlop Tires Operations, S. A. v. Brown, 564

U.S. 915, 919 (2011). “A court with general jurisdiction may hear any claim

against that defendant, even if all the incidents underlying the claim occurred

in a different State.” Bristol–Myers, 137 S.Ct. at 1780. Recently, however,

the United States Supreme Court held that general jurisdiction will not lie in a

state in which neither a parent corporation nor its subsidiary is incorporated

or has its principal place of business. Daimler AG v. Bauman, 571 U.S. 117,

134 S.Ct. 746, 762 (2014). The record does not indicate that any entity within

Ethicon’s corporate hierarchy is incorporated in Pennsylvania or has its

principal place of business in Pennsylvania. Therefore, we need not discuss

general jurisdiction concepts further.

If general jurisdiction does not exist over a foreign defendant, it may

still be subject to specific jurisdiction in Pennsylvania pursuant to

Pennsylvania’s long arm statute, 42 Pa.C.S.A. § 5322 (“Bases of personal

jurisdiction over persons outside this Commonwealth”). Section 5322(a)

contains ten paragraphs that specify particular types of contact with

Pennsylvania deemed sufficient to warrant the exercise of specific jurisdiction.

In addition, Section 5322(b) operates as a “catchall,” providing that

jurisdiction may be exercised over persons who do not fall within the express

provisions of Section 5322(a) to the fullest extent permitted by the Due

Process Clause of the United States Constitution. Mendel v. Williams, 53

A.3d 810, 821 (Pa. Super. 2012) (citation omitted). Regardless, if a

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defendant’s activities in Pennsylvania only give rise to jurisdiction under

section 5322(a) or (b), the plaintiff’s cause of action is limited to those

activities that formed the basis of jurisdiction. See 42 Pa.C.S.A. § 5322(c)

(“when jurisdiction over a person is based solely upon this section, only a

cause of action or other matter arising from acts enumerated in subsection

(a), or from acts forming the basis of jurisdiction under subsection (b), may

be asserted against him”).

Specific jurisdiction enables a court to adjudicate claims arising from

activity that occurs within the forum state’s borders and is “therefore subject

to the State’s regulation.” Bristol-Myers, 137 S.Ct. at 1780. There are three

requirements for the exercise of specific jurisdiction. First, the defendant must

have “purposefully availed itself of the privilege of conducting activities within

the forum State or have purposefully directed its conduct into the forum

State.” Id. at 1785. Second, the plaintiff’s claim must “arise out of or relate

to” the defendant’s activities in the forum state. Id. Third, jurisdiction must

be fair and reasonable so as not to offend tradition notions of fair play and

substantial justice. Id. The fairness factors in the third requirement that a

court will consider are “the burden on the defendant, the forum State’s

interest in adjudicating the dispute, the plaintiff’s interest in obtaining

convenient and effective relief, the interstate judicial system’s interest in

obtaining the most efficient resolution of controversies, and the shared

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interest of the several States in furthering fundamental substantive social

policies.” Id. at 1786.

In Bristol-Myers, a group of plaintiffs, consisting mainly of non-

California residents, filed a mass tort action in California state court alleging

injuries caused by a blood thinner drug called Plavix. Id. at 1778. The

Supreme Court held that California did not have personal jurisdiction over the

defendant with regard to claims of the non-California residents. Id. at 1783.

California did not have general jurisdiction over Bristol–Myers because the

pharmaceutical company was incorporated in Delaware and headquartered in

New York. Id. at 1783-84. Moreover, California lacked specific jurisdiction

because there was no connection to the non-residents’ claims. The non-

residents did not allege they purchased, ingested or suffered harm from Plavix

in California or received treatment for their injuries in California. Id. at 1778.

Nor did they allege that they were prescribed Plavix in California or by

California physicians. Id. The mere fact that California residents were

prescribed Plavix or ingested it in California, or allegedly sustained the same

injuries as the nonresidents, “[did] not allow the State to assert specific

jurisdiction over the nonresidents’ claims.” Id. at 1781.

Moreover, Bristol-Myers’ decision to contract with a California company

to distribute the drug nationally did not provide a sufficient basis for personal

jurisdiction. Id. at 1783. The Court ruled that a defendant’s contract with a

distributor in the forum state is not itself enough to establish personal

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J-A25032-17

jurisdiction in the State. Id. It noted that there was no allegation that the

defendant engaged in relevant acts together with the distributor in California,

or that the defendant was derivatively liable for the distributor’s conduct. Id.

In short, what was needed—and what was missing—was suit-related

conduct, i.e., a connection between the forum and the specific claims at issue,

“principally, an activity or occurrence that takes place in the forum State.”

Id. at 1781. “[A]ll the conduct giving rise to the nonresidents’ claims occurred

elsewhere.” Id. at 1782.

The Court rejected the California Supreme Court’s “sliding scale” theory

establishing personal jurisdiction. Under this approach, “the strength of the

requisite connection between the forum and the specific claims at issue is

relaxed if the defendant has extensive forum contacts that are unrelated to

those claims.” Id. What the California court did “resembles a loose and

spurious form of general jurisdiction.” Id. For specific jurisdiction, a

defendant’s general connections with the forum state are not enough. Id.

The connection between Ethicon and Pennsylvania is considerably

stronger than the connection between Bristol-Myers and California. Ethicon

supervised the design and manufacturing process of pelvic mesh in

Pennsylvania in collaboration with Secant Medical, Inc., a Bucks County

company. Ethicon also worked closely with an Allentown, Pennsylvania

physician, Vincent Lucente, M.D., in developing Prolift. Both of these factors

support the exercise of specific jurisdiction over Ethicon in Pennsylvania.

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J-A25032-17

To elaborate, Hammons claims that she suffered bodily injuries due to

the properties of the mesh that Ethicon used in its transvaginal mesh product,

Prolift. She contends that Ethicon defectively designed and manufactured the

mesh with polypropylene material that was toxic, dense and inelastic.

Because of its defective design, she asserts, the mesh caused scar plating,

erosion of mesh into her pelvic organs, and extensive personal injuries. The

record illustrates that Ethicon worked together with Secant in Pennsylvania to

design, test and manufacture the Prolift mesh.

Three high-level officials of Secant provided affidavits (R.R. 266b-278b)

that Ethicon provided all material specifications for the weaving of mesh at

Secant’s Pennsylvania plant, including specifications concerning the mesh’s

elasticity, mass, and density, the specifications at the center of Hammons’

claims. Ethicon delivered polypropylene filament to Secant in Pennsylvania.

Id. Secant knitted the filament into large rolls of mesh in, and tested samples

for, compliance with Ethicon’s specifications. Id. Ethicon received the rolls

of mesh from Pennsylvania and processed them further. Id. Emails between

Ethicon and Secant officials demonstrate that Ethicon repeatedly

communicated its requirements for mesh design and development,

manufacturing, quality control, testing, and certification to Secant—all issues

central to this litigation. The emails also show that Ethicon employees visited

Secant’s plant in Pennsylvania on multiple occasions to observe the mesh

production process. This evidence establishes an affiliation between

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J-A25032-17

Pennsylvania and Hammons’ cause of action against Ethicon for defective

design of the Prolift device. Bristol-Myers, 137 S.Ct. at 1781.

Trial evidence6 also shows that Ethicon relied heavily on an Allentown,

Pennsylvania gynecologist, Vincent Lucente, M.D., for the development,

study, and marketing of Prolift. N.T., 12/8/15 (AM), at 19-60. Ethicon

retained Dr. Lucente as its investigator for three important clinical studies that

Ethicon funded concerning the outcomes and safety of Prolift mesh: the

Gynemesh PS study of Prolift’s mesh materials, the US TVM study of the Prolift

prototype, and the Lucente IIS study. Hammons’ Trial Exhibits 750, 2299,

3404, 3410, 3416. Dr. Lucente’s role was so important to Ethicon’s

development of Prolift that Ethicon employees traveled to Pennsylvania in

February 2006 to meet with Dr. Lucente for guidance concerning the

marketing and development strategy for Prolift. Id. Dr. Lucente advised it

would be a “disaster” for a woman to need revision surgery with Prolift.

Hammons’ Trial Exhibit 3404. At Ethicon’s behest, Dr. Lucente interceded on

Ethicon’s behalf to persuade the American College of Obstetricians and

Gynecologists to remove a designation of these mesh procedures as

“experimental.” Hammons’ Trial Exhibits 2299, 3416. Ethicon paid Dr.

Lucente over $1.7 million for his services in Pennsylvania, services that were

____________________________________________

6 We may affirm “on any ground.” Wilson v. Plumstead Tp. Zoning
Hearing Bd., 936 A.2d 1061, 1065 n.3 (Pa. 2007). Thus, we need not confine
our reasons for affirming to evidence adduced during proceedings on Ethicon’s
preliminary objections to jurisdiction.

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J-A25032-17

relevant to Hammons’ claims. Hammons’ Trial Exhibit 3404. This evidence

too provides an affiliation between Pennsylvania and Hammons’ design defect

claim, thus permitting exercise of specific jurisdiction over Ethicon in

Pennsylvania. Bristol-Myers, 137 S.Ct. at 1781; see also Cortina, 2017

WL 2793808 at *3 (two pharmaceutical companies were subject to specific

jurisdiction in California based on clinical trials conducted in California that

were relevant to plaintiff’s claims and part of “causal chain” that led to

plaintiff’s injury); Symbolstix, LLC v. Smarty Ears, LLC, 152 F.Supp.3d

1027, 1036 (N.D. Ohio 2015) (in copyright infringement action in Ohio,

specific jurisdiction existed over Texas company that sold educational mobile

device applications, where company’s contacts with speech pathologists in

Ohio were central to its product development and marketing strategies).

For these reasons, the trial court correctly denied Ethicon’s motion to

dismiss this action for lack of personal jurisdiction.7

STATUTE OF LIMITATIONS

Ethicon argues that the trial court erred in denying its post-trial motions

seeking judgment n.o.v. on the ground that Hammons’ action is time-barred

____________________________________________

7 While Ethicon objected to personal jurisdiction, it did not raise any objection
to venue during this case. Venue and personal jurisdiction are different issues.
Personal jurisdiction concerns whether the defendant has engaged in sufficient
activity within Pennsylvania to be subject to this state’s regulation. Venue
concerns whether the forum chosen by the plaintiff (here, Philadelphia
County) is a proper locality within which to bring her action. See Pa.R.Civ.P.
2179 (identifying counties in which venue lies for personal actions against
corporations).

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J-A25032-17

under Indiana’s two-year statute of limitations. Hammons counters that

following her May 2009 surgery, Dr. Baker and Dr. Lackey failed to discover

over the next several years that Prolift caused her injuries, and since these

experienced physicians could not detect the problem, neither could she. She

asserts that she only became aware that Prolift caused her injuries when Dr.

Heit diagnosed the problem on August 30, 2012, less than two years before

May 31, 2013, the date she filed suit.

As an appellate court, we must decide issues such as this by construing

the evidence in the light most favorable to the verdict winner, Hammons.

Construed in this light, the evidence establishes that August 16, 2011 was the

earliest date on which Hammons had notice that Prolift caused her injuries.8

Since this was less than two years before Hammons filed suit, Ethicon’s statute

of limitation argument fails.

There are two bases on which the court can grant judgment n.o.v.:

[O]ne, the movant is entitled to judgment as a matter of law
and/or two, the evidence is such that no two reasonable minds
could disagree that the outcome should have been rendered in
favor of the movant. With the first, the court reviews the record
and concludes that even with all factual inferences decided
adverse to the movant[,] the law nonetheless requires a verdict
in his favor, whereas the second, the court reviews the evidentiary
record and concludes that the evidence was such that a verdict for
the movant was beyond peradventure.

____________________________________________

8 As noted above, August 16, 2011 was the date Hammons signed a form
authorizing the release of her “implant related medical records” for use in
“plaintiff litigation for product liability.” DTX-42; N.T., 12/11/15 (PM), at 63.

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J-A25032-17

Menkowitz v. Peerless Publications, Inc., 176 A.3d 968, 976-77 (Pa.

Super. 2017) (en banc) (citation omitted). In an appeal from the trial court’s

decision to deny judgment n.o.v.,

we must consider the evidence, together with all favorable
inferences drawn therefrom, in a light most favorable to the
verdict winner. Our standard of review when considering motions
for a directed verdict and judgment notwithstanding the verdict
are identical. We will reverse a trial court’s grant or denial of a
judgment notwithstanding the verdict only when we find an abuse
of discretion or an error of law that controlled the outcome of the
case. Further, the standard of review for an appellate court is the
same as that for a trial court.

Id. at 977 (citation omitted).

The Indiana Products Liability Act (“IPLA”) imposes liability upon a seller

for physical harm caused by a “product in a defective condition unreasonably

dangerous to any user or consumer” when:

(1) the user or consumer is in the class of persons that the seller
should reasonably foresee as being subject to the harm caused by
the defective condition;

(2) the seller is engaged in the business of selling the product;
and

(3) the product is expected to and does reach the user or
consumer without substantial alteration in the condition in which
the product is sold by the person sought to be held liable under
this article.

Ind. Code § 34-20-2-1. In an action for design defect, “the party making the

claim must establish that the manufacturer or seller failed to exercise

reasonable care under the circumstances in designing the product.” Ind. Code

§ 34-20-2-2. For purposes of a design defect claim,

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J-A25032-17

[a] product is in a defective condition under [IPLA] if, at the time
it is conveyed by the seller to another party, it is in a condition:

(1) not contemplated by reasonable persons among those
considered expected users or consumers of the product; and

(2) that will be unreasonably dangerous to the expected
user or consumer when used in reasonably expectable ways
of handling or consumption.

Ind. Code § 34-20-4-1.

In an action for failure to provide adequate warnings, a product is

defective if the seller fails to: “(1) properly package or label the product to

give reasonable warnings of danger about the product; or (2) give reasonably

complete instructions on proper use of the product; when the seller, by

exercising reasonable diligence, could have made such warnings or

instructions available to the user or consumer.” Ind. Code § 34-20-4-2. The

plaintiff must show the manufacturer “failed to exercise reasonable care under

the circumstances . . . in providing the warnings or instructions.” Ind. Code

§ 34-20-2-2.

The IPLA provides that the defendant may raise defenses to product

liability claims. Ind. Code §§ 34-20-6-1 and 34-20-6-2. The burden of

proving any defense is upon the defendant. Ind. Code § 34-20-6-2.

Indiana Code § 34-20-3-1 provides that “any product liability action in

which the theory of liability is negligence or strict liability in tort . . . must be

commenced within two (2) years after the cause of action accrues . . .”

Although the statute does not define “accrues,” Indiana courts have adopted

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J-A25032-17

a “discovery rule” under which “the two-year statute of limitations begins to

run from the date the plaintiff knew or should have discovered that she

suffered an injury or impingement, and that it was caused by the product or

act of another.” Degussa Corp. v. Mullens, 744 N.E.2d 407, 410 (Ind.

2001). “[C]ase law regarding medical malpractice claims is instructive” in

Indiana product liability cases, “because medical and diagnostic issues are

common between the two actions, the statute of limitations for both claims is

two years, and discovery is sometimes at issue in determining whether the

respective statutes of limitation have been triggered.” Id.

In Degussa, the leading Indiana case on this subject, the plaintiff

suspected that workplace chemicals caused her persistent cough. On March

17, 1992, her primary care physician diagnosed her with bronchitis and told

her that the cough might have several causes, including the workplace. On

March 26, 1992, a specialist, Dr. Reihman, told the plaintiff that it was possible

that work-related chemical exposure only was triggering an injury caused by

something else. In June 1992, after performing tests, Dr. Reihman observed,

“The etiology of [the plaintiff’s] chronic airflow obstruction and its relationship

to her work environment remains unclear.” At about the same time,

representatives from Degussa Corporation visited the plaintiff at work and told

her that their product could not be causing her medical problems.

Dr. Reihman could not determine the cause of the plaintiff’s problems

and referred her to Dr. Garcia, a pulmonary specialist, for further evaluation.

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J-A25032-17

Dr. Garcia treated Mullens and attempted to diagnose her problems from June

1992 until March 1994, when he informed the plaintiff that her lung disease

was caused by exposure to Degussa’s chemicals in the workplace.

On March 25, 1994, the plaintiff filed suit against Degussa. Degussa

argued that her lawsuit was time-barred because she did not file suit within

two years after March 17, 1992, the date of her first visit with her primary

care physician. The trial court denied Degussa’s motion for summary

judgment, but Indiana’s intermediate Court of Appeals reversed. The plaintiff

appealed to the Indiana Supreme Court, which reversed the Court of Appeals,

and held that the trial court properly denied summary judgment to Degussa,

and remanded for trial. The Supreme Court reasoned:

Although “[e]vents short of a doctor’s diagnosis can provide a
plaintiff with evidence of a reasonable possibility that another’s”
product caused his or her injuries, a plaintiff’s mere suspicion or
speculation that another’s product caused the injuries is
insufficient to trigger the statute. Evenson v. Osmose Wood
Preserving Co. of Am., 899 F.2d 701, 705 (7th Cir.1990)
(applying Indiana law). While [the plaintiff] might have suspected
that a chemical from work was the cause of her problems when
she first visited Dr. Watkins on March 17, 1992, the best that Dr.
Watkins could do to respond to her concerns was to emphasize
that there were a range of potential causes. See id. (“Although
[plaintiff] himself suspected at this time [(the time of his visit to
the doctor and request for CCA chemical tests)] that CCA was the
culprit, his attempts to determine the actual cause were rebuffed
by his doctors in whom he could place some reliance. What
[plaintiff] had ... was not some evidence of a reasonable possibility
that CCA was the cause but only a layman’s mere suspicion to this
effect.”)

Circumstances where a physician tells a patient that a product or
act is one of several “possible” causes of an injury present a
complex of factually and legally relevant questions about how the

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J-A25032-17

physician conveyed the information to the patient and what
emphasis the physician placed on the potentially tortious cause
over other causes. Nevertheless, [the plaintiff] was responsible
and diligently followed her physician’s recommendations,
undergoing further tests and attempting to gather information
regarding the cause of her medical problem and its relationship to
past respiratory ailments before initiating a lawsuit against
Defendants. [The plaintiff] attempted to gather information that
would transform speculation into a causal link that was
“reasonably possible” or “probable” before she filed suit against
Defendants.

On March 17, 1992, [the plaintiff] merely suspected that work
products had something to do with her illness and Dr. Watkins
said nothing to confirm, deny, or even strengthen her suspicions.
In light of the ongoing medical consultation that [the plaintiff]
undertook between March 17, 1992, and March 25, 1994, the date
[the plaintiff] filed her complaint, we do not believe that the
statute was triggered as late as March, 1994, as argued by [the
plaintiff]. However, we also see nothing in the record to indicate
that on March 17, 1992 (or even in the following eight days that
would have been outside of the statutory period), [the plaintiff]’s
physicians had yet informed her that there was a reasonable
possibility, if not probability, that her ailments were caused by
work chemicals.

Id., 744 N.E.2d at 411-12.9 “A reasonable possibility, while less than a

probability, requires more than . . . mere suspicion.” Evenson, 899 F.2d at

705. The discovery rule is objective in nature—that is, the test is not what

Hammons knew or suspected, but what would have caused a person of

reasonable diligence to take action that would lead to the discovery of her

____________________________________________

9 The trial court stated incorrectly that a claim accrues when the treating
physician informs the patient of the “probability” that her injury was caused
by an act or product of another. Trial Court Opinion, at 8. We apply the
proper “reasonable possibility” standard below.

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J-A25032-17

cause of action. Anonymous Physician v. Wininger, 998 N.E.2d 749, 751-

52 (Ind. App. 2013); Morgan v. Columbus McKinnon Corp., 837 N.E.2d

546, 550 (Ind. App. 2005).

When the defendant raises the statute of limitations as an affirmative

defense, the defendant bears the burden of establishing that the plaintiff filed

her action beyond the limitation period. McDaniel v. Erdel, 91 N.E.3d 617,

624 (Ind. App. 2017). If the defendant fulfills this burden, the burden shifts

to the plaintiff to establish “an issue of fact material to a theory that avoids

the defense,” id., such as the discovery rule.10 The court can resolve a

discovery rule issue as a question of law when no material issues of fact are

in dispute. Kerr v. City of South Bend, 48 N.E.3d 348, 353 (Ind. App.

2015).11 When issues of fact remain in dispute, the jury should resolve the

discovery rule question. Allied Resin Corp. v. Waltz, 574 N.E.2d 913, 915

(Ind. 1991). When the jury returns a verdict in favor of the plaintiff, the

burden shifts back to the defendant at the post-trial stage. To obtain

____________________________________________

10 Pennsylvania law provides the same shifting burden of proof. A defendant
asserting an affirmative defense such as the statute of limitations has the
initial burden of proof as to that affirmative defense. Sabella v. Appalachian
Development Corp., 103 A.3d 83, 93 (Pa. Super. 2014). When the
defendant meets this burden, the burden shifts to the party relying on the
discovery rule as a rejoinder to the statute of limitations defense. Wilson v.
El-Daief, 964 A.2d 354, 362 (Pa. 2009).

11 Pennsylvania law is the same. See Nicolau v. Martin, 153 A.2d 383, 395
(Pa. Super. 2016) (en banc) (affirming summary judgment in medical
malpractice case where plaintiff failed as matter of law to raise genuine issue
of fact as to applicability of discovery rule).

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J-A25032-17

judgment n.o.v., the defendant must demonstrate that even with all factual

inferences decided against it, the law nonetheless requires a verdict in its favor

on the discovery rule issue. Menkowitz, 176 A.3d at 976-77.

Hammons commenced this action on May 31, 2013. To obtain judgment

n.o.v. on its statute of limitations defense, Ethicon had to demonstrate, as a

matter of law, that the evidence provided a person of reasonable diligence

with a “reasonable possibility” before May 31, 2011 to believe that Prolift

caused Hammons’ injuries. Degussa, 744 N.E.2d at 411. The evidence does

not support this result.

Hammons presented evidence that after her implant surgery on May 5,

2009, she visited Dr. Baker five times over the next few months and reported

pelvic pain and urinary and sexual dysfunction. Dr. Baker never attributed

these symptoms to Prolift; in fact, he gave her no answers at all. Hammons

testified:

Q. So when you went to see Dr. Baker and you and Mr. Wilson
had tried to engage in intercourse and it was painful for you, when
you went to see Dr. Baker, you told him about that; is that right?

A. Yes, I did.

Q. And I understand you feel as if he wasn’t responsive to you.
He couldn’t give you any answers; is that correct?

A. That’s right.

N.T., 12/11/15 (P.M.), at 34; see also id. at 36 (“I told him that we couldn’t

have [a sexual] relationship. I asked him how come I couldn’t have sex? And

he never did answer me”). Hammons’ expert, Ralph Zipper, M.D., reviewed

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J-A25032-17

notes of her treating physicians and explained that Dr. Baker’s notes did not

indicate awareness that the symptoms were mesh-related. Instead, Dr. Baker

noted that Hammons’ surgery and post-operational healing went very well,

and he observed “no erosion.” When Hammons returned with complaints of

pelvic pain, incontinence, and sexual dysfunction, Dr. Baker offered no

explanation and recommended waiting for additional recovery before

engaging in sexual intercourse. N.T., 12/11/15 (P.M.) at 97-102; N.T.,

12/10/15 (A.M.) at 37-52; P-3418 at 15-20.

Hammons visited Dr. Lackey after Dr. Baker failed to offer a remedy,

and Dr. Lackey diagnosed rectocele (rectal prolapse), pelvic pressure and pain

with intercourse. On December 15, 2009, he surgically repaired the rectocele

with Hammons’ own tissue. His post-operative note did not mention the Prolift

device; nor was he aware that the product implanted in Hammons was from

Prolift. On January 28, 2010, Dr. Lackey cleared Hammons to resume sexual

intercourse. It does not appear that Hammons visited Dr. Lackey again (or

another physician) before May 31, 2011.

Accepting this evidence as true, we hold that the trial court properly

denied judgment n.o.v. on the statute of limitations issue. The parties hotly

disputed whether Hammons knew, or should have known through the exercise

of reasonable diligence, that her symptoms were a manifestation of injury

caused by Prolift, as opposed to, or in addition to, the typical condition that

surgery produces. Ethicon argued that a reasonable person in Hammons’

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J-A25032-17

position would have realized the possibility that Prolift was to blame, given

her prolonged and persistent post-surgical pain and incontinence. The

evidence shows, however, that as of January 28, 2010, two experienced

gynecologists failed to diagnose Prolift as the cause of her injuries. Since they

failed to draw a nexus between Prolift and Hammons’ injuries, the jury could

conclude that it was reasonable for Hammons not to have drawn any

connection. Nor does the record include any fact between January 28, 2010

and May 31, 2011 that placed Hammons on notice that Prolift caused her

injuries. Although we recognize that “events short of a doctor’s diagnosis can

provide a plaintiff with evidence of a reasonable possibility that another’s

product caused her injuries,” Degussa, 744 N.E.2d at 411, we do not see any

events here that established this possibility as a matter of law prior to the

limitation period. It was proper for the jury to resolve this fact-sensitive

question.

Ethicon argues that on August 16, 2011, Hammons signed a form

authorizing the release of Hammons’ “implant related medical records” for use

in “plaintiff litigation for product liability.” DTX-42; N.T., 12/11/15 (PM), at

63. This language, Ethicon contends, established a “reasonable possibility” as

of this date that Prolift was the cause of her injuries. Degussa, 744 N.E.2d

at 411. This alone, however, did not entitle Ethicon to judgment n.o.v.

because less than two years elapsed between August 16, 2011 and the date

Hammons filed this lawsuit, May 31, 2013.

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J-A25032-17

Recognizing this fact, Ethicon argues that the authorization form

demonstrates the existence of a “reasonable possibility” more than two years

before Hammons filed suit, because Hammons “identifies no . . . new facts

that allegedly put her on notice after her apparent and persistent symptoms

in 2009 but before the August 16, 2011 release of records.” Ethicon’s Reply

Brief at 14 (emphasis in original). We disagree. As discussed above, viewed

in the light most favorable to the verdict winner, Hammons, the evidence

demonstrates the jury could conclude that as of January 28, 2010, the date

Dr. Lackey cleared Hammons to resume sexual intercourse, she was not on

notice of a “reasonable possibility” that Prolift caused her injuries. Further,

contrary to Ethicon’s argument, Hammons did not have the burden at the

post-trial stage to disprove that some “new fact” put her on notice “before the

August 16, 2011 release of records.” Instead, Ethicon had the burden at the

post-trial stage to identify this “new fact” in the record. Ethicon has not met

this burden. Based on the language in the release form, Ethicon speculates

that Hammons could not suddenly have had an epiphany about Prolift on

August 16, 2011. She had to have realized earlier that something was wrong

with the device. But when did she arrive at this realization? The record does

not say. Without some fact of record that proves notice arose before May 31,

2011, Ethicon cannot obtain judgment n.o.v. on the statute of limitations

issue.

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J-A25032-17

ADEQUACY OF WARNINGS

Ethicon argues that it is entitled to judgment n.o.v. because Hammons

failed to prove that Ethicon’s warnings were inadequate. We disagree.

As stated above, Hammons had the duty to prove that Ethicon failed to

“(1) properly package or label the product to give reasonable warnings of

danger about the product; or (2) give reasonably complete instructions on

proper use of the product; when [Ethicon], by exercising reasonable diligence,

could have made such warnings or instructions available to the user or

consumer.” Ind. Code § 34-20-4-2.

The duty to warn arises because a product manufacturer should have

superior knowledge of its product. Nat. Gas Odorking, Inc. v. Downs, 685

N.E.2d 155, 163 (Ind. App. 1997). Because “the injured person is helpless to

protect himself from the actually defective product, it is only reasonable

therefore that as between the injured user and the one who places the product

on the market the latter should bear the loss.” Ortho Pharm. Corp. v.

Chapman, 388 N.E.2d 541, 548 (Ind. App. 1979). A manufacturer may not

delegate its duty to warn. Nat. Gas Odorking, 685 N.E.2d at 163 & n.10.

Indiana follows the learned intermediary doctrine, under which Ethicon’s

duty to warn for a prescription-only product like Prolift “extends only to the

medical profession, and not the ultimate users.” Ortho Pharm. Corp., 388

N.E.2d at 548-59. A manufacturer “ha[s] no duty to warn with respect to

such potential [risks] . . . already known to the user, the operating surgeon,”

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J-A25032-17

or those risks about which the surgeon should know. Phelps v. Sherwood

Med. Indus., 836 F.2d 296, 300, 303-04, 305 (7th Cir. 1987).

To determine whether a manufacturer has satisfied its duty to warn by

relying upon a sophisticated intermediary, courts should consider the following

factors:

[T]he likelihood or unlikelihood that harm will occur if the
[intermediary] does not pass on the warning to the ultimate user,
the trivial nature of the probable harm, the probability or
improbability that the particular [intermediary] will not pass on
the warning and the ease or burden of the giving of the warning
by the manufacturer to the ultimate user.

Nat. Gas Odorking, 685 N.E.2d at 163. Further, for the exception to apply,

“the intermediary must have knowledge or sophistication equal to that of the

manufacturer or supplier, and the manufacturer must be able to rely

reasonably on the intermediary to warn the ultimate consumer.” Id. at 164.

Reliance is only reasonable if the intermediary knows or should know of the

product’s dangers. Id. Actual or constructive knowledge may arise where

either the supplier has provided an adequate explicit warning of such dangers

or the information of the product’s dangers is available in the public domain.

Id. Of note here,

whether a manufacturer has discharged its duty under the
sophisticated intermediary doctrine is almost always a question
for the trier of fact. The manufacturer’s reliance on the
intermediary’s alleged sophistication may be more or less
reasonable given the product’s nature, complexity and associated
dangers, the likelihood that the intermediary will communicate
warnings to the ultimate consumer, the dangers posed to the
ultimate consumer by an inadequate or nonexistent warning, and
the feasibility of requiring the manufacturer to directly warn the

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J-A25032-17

product’s ultimate consumers. Ultimately, those factors must be
balanced by the trier of fact.

Id.

With these standards in place, we turn to the evidence adduced during

trial. Viewed in the light most favorable to Hammons, the verdict winner, the

evidence shows that at the time of Prolift’s product launch in March 2005,

Ethicon was aware of serious risks caused by Prolift but failed to make these

risks clear in its indications for use (“IFU”) and patient brochures.

In March 2005, Ethicon began marketing Prolift. Concurrent with this

product launch, Ethicon issued an IFU which stated:

WARNINGS AND PRECAUTIONS

****

Post-operatively the patient should be advised to refrain from
intercourse, heavy lifting and/or exercise (e.g. cycling, jogging)
until the physician determines when it is suitable for the patient
to return to her normal activities.

Avoid placing excessive tension on the mesh implant during
handling.

****

The GYNECARE PROLIFT Pelvic Floor Repair Systems should be
used with care to avoid damage to vessels, nerves, bladder and
bowel. Attention to patient anatomy and correct use of the device
will minimize risks.

Transient leg pain may occur and can usually be managed with
mild analgesics.

Do not manipulate the GYNECARE PROLIFT Retrieval Device with
sharp instruments or cut it to alter its length.

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J-A25032-17

ADVERSE REACTIONS

Potential adverse reactions are those typically associated with
surgically implantable materials, including infection potentiation,
inflammation, adhesion formation, fistula formation, erosion,
extrusion and scarring that results in implant contraction.

Punctures or lacerations of vessels, nerves, bladder, urethra or
bowel may occur during GYNECARE PROLIFT Guide passage and
may require surgical repair.

P-1005, at 5-6; P-1010.

Ethicon’s Prolift brochures used similar language, calling the risks “rare.”

Ethicon encouraged women to make their own decisions regarding prolapse,

without providing any information concerning the crucial risks associated with

the product, but warning only about the risks of surgery:

What are the risks? All surgical procedures present some risks.
Although rare, complications associated with the procedure
include injury to blood vessels of the pelvis, nerve damage,
difficulty urinating, bladder and bowel injury. There is also a small
risk of the mesh material becoming exposed into the vaginal
canal.

P-2881 at 6-8. The purpose of the patient brochure was to facilitate

discussions between the patient and her physician about the benefits and risks

of the Prolift system. P-3415, at 458-59.

The IFU and brochures failed to disclose the full extent of the risks posed

by Prolift—risks that Ethicon knew about prior to the March 2005 product

launch. In November 2004, French surgeons who had been using the Prolift

kit for several years published an article addressing Gynemesh Soft, the same

mesh material used in the Prolift system, opining that retraction was

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impossible to forecast and highly variable and that its after-effects included

dyspareunia (painful sexual intercourse). On January 11, 2005, before the

product launch of the Prolift kit, Axel Arnaud, the scientific director of

Gynecare Europe, sent an email to Ophelie Berthier, the product director who

oversaw the marketing launch of Prolift worldwide, proposing to add the

following warning to the IFU:

Warning: Early clinical experience has shown that the use of mesh
through a vaginal approach can occasionally/uncommonly lead to
complications such as vaginal erosion and retraction, which can
result in an anatomical distortion of the vaginal cavity that can
interfere with sexual intercourse. Clinical data suggests the risk of
such a complication is increased in cases of associated
hysterectomy. This must be taken in consideration when the
procedure is planned in a sexually active woman.

P-3401, at 566-68. Berthier advised it was urgent to incorporate the changes

in the IFU version in the procedure CD–ROM. Berthier’s email was forwarded

to Charlotte Owens, M.D., Ethicon’s worldwide medical director at the time of

the product launch in 2005, and Sean O’Bryan, Ethicon’s senior project

manager for regulatory affairs, along with a question whether it was

acceptable to add this warning without FDA approval. On January 13, 2005,

O’Bryan responded that he would leave it to Owens and Arnaud to decide. P-

3412, at 146. Scott Ciarrocca, the project’s research and development project

leader, replied several minutes later, “We have already printed launch stock.

This would be a next revision addition, but they want it in there ASAP.” Id.

at 148. Thus, Ethicon rejected Arnaud’s suggestion because incorporating it

into the IFU would require replacing the previously printed IFU’s, thus

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incurring additional costs and delaying the product launch. Id. at 148, 154-

55.

Owens testified that she understood the IFU had to be clear,

unambiguous, accurate, and supported by data, and she claimed the IFU

communicated all contraindications, warnings, precautions, and adverse

reactions to physicians. P-3413, at 260-62. Owens acknowledged that she

approved the IFU even though she knew there might be long-term

complications. Id. at 254-55. On January 14, 2005, Owens issued a clinical

expert report to document the safety and functionality of the Prolift system to

treat pelvic floor repair. She relied on a Gynemesh PS clinical study performed

by physicians using Gynemesh PS for vaginal and abdominal placements. Her

report on Prolift listed the same potential complications identified in the

Gynemesh PS study, such as “[i]nfection, mesh exposure, fistula, hematoma,

and contraction.” P-3413, at 197-99. She reported there were no instances

of tissue contraction in the Gynemesh clinical evaluation. Id. But at the time

Owens authored this clinical expert report, she was familiar with the 2004

article published by the French surgeons that identified retraction as a

potential complication along with such aftereffects as severe pain. Owens did

not cite the French surgeons’ article in her report or discuss the possibility of

retraction. Id. She admitted that before Prolift’s market launch, she knew

the mesh could erode, migrate, or lead to inflammation, and that removal of

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mesh could be very difficult even though Ethicon did not conduct studies on

how to remove it. Id. at 310-312.

Likewise, Piet Hinoul, M.D.—an urogynecologist who joined Gynecare in

2008 as a worldwide medical director—confirmed that on the day of the launch

Ethicon was aware of potential complications, such as urinary incontinence,

urinary retention or obstruction, ureteral obstruction, voiding dysfunction,

pain, pelvic pain, and pain with intercourse. P-3404, at 382-83.

Dr. Elliott, one of Hammons’ expert witnesses, reviewed Ethicon’s IFU,

sales brochures, and internal documents and testified that Ethicon’s warnings

were inadequate because they failed to convey Prolift’s full risk profile,

namely, “all the known complications, their severity, their frequency.” He

explained that by May 2009, Ethicon knew Prolift posed significant risk to

women on various issues: chronic, severe, and progressive inflammation;

failure to integrate into tissue; scar plate and fibriotic bridge formation;

excessive mesh contraction; pain during sexual activity and ambulation;

recurrent exposure of mesh; chronic pelvic floor muscle spasms; chronic

urinary and sexual dysfunction; and additional surgeries for mesh removal.

P-3401 at 3-9, 18-20; P-3402 at 37-48; P-3403, at 5-7; P-3404, at 12-17; P-

3413 at 6-10; P-3415 at 2-6.

Dr. Klinge, another expert witness for Hammons, testified that

physicians are “dependent on the information that is provided by the

manufacturer for the long-term risks or for the risks that are connected to

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th[e] device. There is no other way to get this information.” P-3408. The

medical device manufacturer has the duty to warn treating physicians about

serious adverse events caused by the device so that the physician can have

an appropriate risk-benefit discussion with the patient. P-3408 at 203-09.

Testimony from other Ethicon employees revealed that Ethicon

controlled information that reached physicians through other channels.

Ethicon trained physicians on Prolift implantation but educated them only

about risks disclosed in the IFU. Ethicon also controlled the message in

published medical literature and diluted input from independent clinicians on

the safety and efficacy of Prolift. P-3414 at 2; P-3416 at 1-7.

The evidence shows that Ethicon failed to disclose the risks inherent in

Prolift to Dr. Baker, who implanted the Prolift device. Dr. Baker testified he

depended upon Ethicon for information about Prolift’s risks, and that he relied

upon Ethicon’s IFU and brochures to recommend Prolift to Hammons. In 2006,

Dr. Baker received training from Ethicon to perform the procedure. He had

no other independent knowledge of Prolift’s risks or performance. Dr. Baker

stated that had he known about the high risk of severe and permanent

complications from Prolift, he would not have offered it to Hammons. P-3418

at 2-26. Dr. Elliott testified that Ethicon should have “absolutely” included

these warnings in the IFU. He added that Prolift is not appropriate for most

women, but only those with high-grade recurring prolapse. He testified that

the IFU and marketing documents affirmatively misled treating physicians,

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because it warned of only minimal inflammatory reaction, normal healing,

limited scarring, rare complications and transient pain. The IFU

misrepresented that Prolift did not degrade and remained. P-3401 at 7-8; P-

3402 at 37-52; P-3408 at 15-17; P-3409 at 2-7.

Viewed in the light most favorable to Hammons, the verdict winner, this

evidence establishes that Ethicon failed to provide adequate warnings to Dr.

Baker about the risks of Prolift, and that Dr. Baker neither knew nor should

have known independently about these risks. Ethicon led Dr. Baker to believe

that the risks of the device were not nearly as serious as they actually were.

As a result, he did not convey the full extent of the risks to Hammons.

Ethicon argues that Dr. Baker’s notes following Hammons’ initial surgery

in 2009 demonstrate that he fully advised her of the risks: “I discussed the

. . . risk of injury to bowel, bladder or ureter as well as . . . having pain with

intercourse or other types of pain following surgery. [Hammons] agreed to

these risks . . .” DTX-37 at 208-09. In making this argument, Ethicon

construes the evidence in the light most favorable to itself instead of in the

light most favorable to Hammons, the correct standard. Ethicon ignores

Hammons’ testimony that Dr. Baker did not inform her of the risks and Dr.

Baker’s testimony that Ethicon did not advise him of the extent of the risks

posed by Prolift. Moreover, Ethicon failed to establish, as a matter of law, that

Dr. Baker was on constructive notice of Prolift’s risks, i.e., that he should have

realized the risks even if Ethicon failed to expressly identify them. As a result,

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he could not convey to Hammons the severe and permanent risks of the

device. He would not have recommended the device to Hammons had he

known of the actual risks.

There was sufficient evidence for the duty to warn issue to go to the

jury in this case. The jury was free to determine, as it did, that Ethicon

violated its duty to warn Hammons’ physician about the risks of Prolift. The

trial court properly denied Ethicon’s motion for judgment n.o.v. on this issue.

SAFER ALTERNATIVE DESIGN

In its next two arguments, Ethicon asserts that (1) Hammons’ design

defect claim fails as a matter of law, thus entitling Ethicon to judgment n.o.v.,

because Hammons failed to prove the existence of a feasible safer alternative

design, and (2) the trial court erred by failing to instruct the jury that

Hammons was required to prove that a safer alternative design was available.

We disagree with both arguments. The IPLA does not require proof of a safer

alternative design. Even if it did, Hammons provided evidence that a safer

alternative design existed during the relevant time period in this case.

Earlier this year, the United States District Court for the Northern District

of Indiana, Hammond Division, comprehensively discussed this issue in

another action against Ethicon involving Prolift, Kaiser v. Johnson &

Johnson, 2018 WL 739871 (N.D. Ind., Feb. 7, 2018). The district court’s

excellent analysis deserves recitation.

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J-A25032-17

The district court began by describing the original version of the IPLA

and important amendments to this act in 1995:

In 1978, the Indiana Legislature enacted the IPLA. At the time,
the IPLA provided that it “govern[s] all products liability actions,
including those in which the theory of liability is negligence or
strict liability in tort; provided however, that this chapter does not
apply to actions arising from or based upon any alleged breach of
warranty.” Ind. Code § 33-1-1.5-1 (1978). While the IPLA
codified most aspects of the Restatement (Second) on Torts
§ 402A regarding strict liability, it spoke nothing of the treatment
of actions sounding in negligence. As a result, the IPLA left claims
based on negligence to the common law. See Corbin v. Coleco
Industries, Inc., 748 F.2d 411, 416–17 (7th Cir. 1984)
(discussing the history of the IPLA). In 1983, the IPLA was
amended, removing the reference to negligence actions,
presumably recognizing the confusion that was created by the
Indiana Legislature in 1978. See Ind. Code § 33-1-1.5-1 (1983)
(“[T]his chapter governs all actions in which the theory of liability
is strict liability in tort.”); Miller v. Todd, 551 N.E.2d 1139, 1143
(Ind. 1990) (discussing the history of the IPLA); Moore v.
Sitzmark Corp., 555 N.E.2d 1305, 1308 (Ind. App. 1990) (“[A]n
action [for negligent design] is not subject to the terms of the
Indiana Product Liability Act; rather, it is a common law action.”).

In 1995, the IPLA was amended yet again. The idea was to bring
all product liability actions under one umbrella. The 1995 version
specifically applies to “all actions brought by a user or consumer
against a manufacturer or seller for physical harm caused by a
product regardless of the substantive legal theory or theories upon
which the action is brought.” See Ind. Code § 33-1-1.5-1 (1995);
P.L. 278-1995, Sec. 1 (effective July 1, 1995). The 1995
amendments brought some much needed clarity to product
liability cases in Indiana by eliminating strict liability claims for all
design defect and failure to warn claims and instead imposing a
negligence standard in all such cases. It did so by adding the
“reasonable care” language, quoted above, that remains in effect
today. See Ind. Code § 33-1-1.5-3 (1995); P.L. 278-1995, Sec.
1 (effective July 1, 1995). In 1998, the IPLA was amended once
more, but this amendment did nothing more than move the IPLA
to Title 34. See Ind. Code §§ 34-20-1-1 to 34-20-9-1.

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What this history shows us is that, until 1995, the standard for
product liability claims sounding in negligence was established by
the common law. During that time, the Courts held that, under
Indiana law, a plaintiff “must offer a safer, more practicable
product design than the design in question” to succeed on a
negligent design defect claim. Whitted v. General Motors
Corp., 58 F.3d 1200, 1206 (7th Cir. 1995) (citing Miller v. Todd,
551 N.E.2d 1139, 1143 (Ind. 1990)). Therefore, until July 1,
1995, a plaintiff was required to show that a safer alternative
design to succeed on a negligent design defect claim.

I cite to Whitted for this explanation quite intentionally. It was
decided on June 29, 1995, before the 1995 amendments
establishing the negligence standard for design defect and failure
to warn cases went into effect. Yet Whitted, or in a few
circumstances its contemporaries or progeny, is the case relied
upon in most of the authority on which Ethicon relies for its
assertion that proof of safer alternative design continues to be a
required element of a negligent design defect claim. See, e.g.,
Simmons v. Philips Elec. N. Am. Corp., No. 2:12–CV-39-TLS,
2015 WL 1418772 (N.D. Ind. Mar. 27, 2015) (quoting Whitted);
Hathaway v. Cintas Corp. Serv. Inc., 903 F. Supp. 2d 669, 675
(N.D. Ind. 2012) (quoting Whitted); McClellon v. Thermo King
Corp., 2013 WL 6571946, at *10 (S.D. Ind. 2013) (quoting
Whitted and citing Barnard v. Saturn Corp., a Div. of General
Motors Corp., 790 N.E.2d 1023, 1032 (Ind. App. 2003), which
relies on a 1989 Indiana Court of Appeals case applying the old
statute); Hartman v. EBSCO Industries, Inc., 2013 WL
5460296, at *7 (N.D. Ind. 2013) (quoting Rodefer v. Hill’s Pet
Nutrition, Inc., No. IP 01–123–C H/K, 2003 WL 23096486, at *9
(S.D. Ind. Nov. 7, 2003), which cites Whitted). In fact, it appears
that all of the authority cited by Ethicon in support of its argument
that a safer alternative design is a prima facie element of a
negligent design defect claim traces back to pre-1995 amendment
to the IPLA.

Kaiser, 2018 WL 739871, at *3-4.

The district court then explained that the Indiana Supreme Court held

in 2010 that the IPLA did not require proof of a safer alternative:

Admittedly, the Indiana Legislature was not particularly clear in
1995 regarding whether it intended to completely do away with

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the safer alternative design requirement. As a result, many
federal and state courts in Indiana held course and continued to
require it as an element of a plaintiff’s negligent design defect
claim. But matters changed in 2010 when the Indiana Supreme
Court finally addressed the issue. In TRW Vehicle Safety
Systems, Inc. v. Moore, 936 N.E.2d 201 (Ind. 2010), the
plaintiff brought a negligent design defect claim, among others,
against the defendant seatbelt manufacturer, TRW, and the
defendant vehicle manufacturer, Ford, after the plaintiff’s
decedent was ejected through the sunroof of his vehicle when his
seatbelt developed slack in a rollover that followed a tire failure.
TRW Vehicle Safety Systems, Inc., 936 N.E.2d at 208. The
jury apportioned 5% of the fault to TRW and 31% of the fault to
Ford. Id. The Court of Appeals reversed, finding insufficient
evidence to support the jury’s verdict. Id. The Indiana Supreme
Court disagreed.

Ford and TRW argued that the evidence presented at trial was
insufficient because it failed to establish the requisite standard of
care and prove that their conduct fell below that. Id. at 208-209.
Specifically, they argued that plaintiff failed to present evidence
of the proper standard of care, to offer testing, data, studies, or
other evidence to show a safer, more practicable product design,
and to rebut evidence that its proposed alternative design itself
presented safety concerns. Id. at 209. In response, the Indiana
Supreme Court explained:

The [IPLA] generally imposes strict liability for
physical harm caused by a product in an unreasonably
dangerous defective condition. Ind. Code § 34–20–
2–1. For actions based on an alleged product design
defect, however, the Act departs from strict liability
and specifies a different standard of proof: ‘[T]he
party making the claim must establish that the
manufacturer or seller failed to exercise reasonable
care under the circumstances in designing the
product.’ Ind. Code § 34–20–2–2. Thus the statute
itself prescribes the applicable standard of care. We
decline to require proof of any additional or more
particular standard of care in product liability actions
alleging a design defect.

Id. at [209]. The opinion included a footnote at the end of the
last sentence that reads:

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J-A25032-17

The American Law Institute recommends a different
approach, prescribing specific sub-elements of a claim
for strict product liability based on design defect. It
views a product as ‘defective in design when the
foreseeable risks of harm posed by the product could
have been reduced or avoided by the adoption of a
reasonable alternative design by the seller or other
distributor, or a predecessor in the commercial chain
of distribution, and the omission of the alternative
design renders the product not reasonably safe.’
Restatement (Third) of Torts: Products Liability § 2(b)
(1997). Our legislature did not adopt this analytical
framework but instead enacted in 1998 a negligence
standard for product liability claims based on defective
design. See Ind. Code § 34–20–2–2.

Id. at 209 n.2. The Indiana Supreme Court, therefore, plainly
held that proof of alternative design is not required under Indiana
law. It may, however, be probative evidence of the defendant’s
use of reasonable care. Id. at 209.

Id. at *4-5.

The district court concluded that it was bound to apply the Indiana

Supreme Court’s decision in TRW, and that other decisions to the contrary

rested on outdated common law:

One would think that TRW put to bed the question of whether,
under Indiana law, a safer alternative design is a necessary
element of a design defect claim. But in the eight years that
followed that decision, many state and federal courts in Indiana
continued to find that proof of alternative design is required for a
design defect claim, citing to Whitted or its progeny in support of
that assertion. These courts are, therefore, relying on outdated
common law, which was superseded by the negligence standard
spelled out in the 1995 amendments to the IPLA as confirmed by
the Indiana Supreme Court in TRW . . . [T]he Indiana Supreme
Court could not have been any clearer in TRW in holding that
proof of an safer alternative design is not required under the IPLA.
As the Indiana Supreme Court correctly pointed out in TRW, the
Indiana Legislature could have adopted the standard set out in the

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J-A25032-17

Restatement (requiring proof of safer alternative design), but it
chose not to. TRW Vehicle Safety Systems, Inc., 936 N.E.2d
at 209 n.2. It has not chosen to amend that language to add in a
safer alternative design requirement in the eight years since the
Indiana Supreme Court decided TRW.

What nails the point home that proof of a safer alternative design
is not required under Indiana law is the fact that the Indiana Model
Civil Jury Instructions do not say a single thing that suggests that
proof of a safer alternative design is an element of a negligence
product liability claim. See Indiana Model Civil Jury Instruction
2305. One would think that if proof of a safer alternative design
was required in Indiana design defect cases, the Indiana Model
Civil Jury Instructions would reflect that fact. Yet they don’t say
boo about it.

Other courts have read TRW in the same way as I do. In
Hammons v. Ethicon, Inc. et al., No. 1305003913, 2016 WL
6821815 (Pa. Com. Pl. Sept. 30, 2016),12 a case involving an
Indiana woman implanted with Ethicon’s Prolift device, the Court
of Common Pleas of [Philadelphia County] held that proof of an
alternative design is not a required element under Indiana law.
Citing and quoting TRW, that court ultimately held that, under
Indiana law, “[t]estimony of an alternative design can be
probative evidence as to the issue of the defendant’s failure to use
reasonable care and can support a reasonable inference of
negligent design but is not [a] requirement.” Hammons, 2016
WL 6821815 at *5.

Likewise, in Bailey v. Cottrell, Inc., 721 S.E.2d 571 (Ga. Ct. App.
2011), a Georgia case interpreting Indiana law, the court held that
Indiana specifically has rejected a risk utility test in favor of a
common law negligence analysis. One of the factors under the risk
utility test is whether there is a safer alternative design. But as
the Georgia Court of Appeals recognized, the risk utility test was
jettisoned in Indiana in favor of a straight-forward negligence
approach. In arriving at that conclusion, the Georgia court cited
to the Indiana Supreme Court’s analysis in TRW and its explicit
rejection of the Restatement (Third) of Torts: Products Liability
§ 2(b) (1997). Bailey, 721 N.E.2d at 374-75 (citing TRW
Vehicle Safety Systems v. Moore, 936 N.E.2d at 209, n.2.).
____________________________________________

12 This, of course, is the trial court’s opinion in the case before us.

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While the road to TRW admittedly was rocky, and confusion still
remains in this state, I believe that the Indiana Supreme Court
has made itself clear. As a result, I agree with the Kaisers that
proof of safer alternative design is not a prima facie requirement
of their case. To hold otherwise would be in contradiction of the
clear Indiana Supreme Court precedent established in TRW, to
which I am bound.

Id. at *5-*6. We agree with Kaiser’s thorough analysis and hold that the

IPLA does not require proof of a safer alternative design.

As it did in Kaiser, Ethicon relies on pre-TRW decisions that rest on

outdated common law and on post-TRW decisions that rely on pre-TRW

cases. Ethicon also attempts to downplay footnote 2 in TRW as “[doing] little

other than not[ing] that Indiana had yet to adopt the Restatement (Third) of

Torts.” Ethicon’s Reply Brief at 20. Ethicon overlooks the precept that the

Indiana Supreme Court is “mindful of both what [a statute] ‘does say’ and

what it ‘does not say.’” Indiana Alcohol and Tobacco Commission v.

Spirited Sales, LLC, 79 N.E.3d 371, 376 (Ind. 2017) (citation omitted). The

Supreme Court’s purpose in footnote 2 of TRW was to show what the 1995

amendment to the IPLA did not say—that is, the legislature excluded “safer

alternative” language to signify its rejection of this element.

Even if a “safer alternative” was necessary, Hammons introduced

evidence that such a product was available, the Prolift+M kit. In January

2005, before Prolift’s product launch, Ethicon engineer Gene Kammerer

suggested the possibility of using Ultrapro mesh for pelvic floor repair in place

of Gynemesh. In an email dated April 13, 2005, he wrote that surgeons and

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customers wanted a better mesh to reduce contraction and scar tissue and

that Ultrapro would make the procedure better for patients and give Ethicon

a significant advantage over the competition. Kammerer said Ultrapro had a

lower inflammatory response, left behind less material than Prolene Soft, and

had a larger pore size than Gynemesh PS to better allow the ingrowth of tissue

and reduce the risk of scar plating and contraction. Over the next four years,

Ethicon developed Ultrapro mesh for pelvic floor repair, which it marketed as

the Prolift+M Pelvic Floor Repair System. One of Prolift’s inventors, Dr.

Cosson, developed the Ultrapro mesh before Hammons’ initial implant

surgery. N.T., 12/7/15 (A.M.), at 57-95; N.T., 12/7/15 (P.M.), at 237-48; P-

3401 at 2-3; P-3404 at 9; P-3407 at 4, 12; P-1318, 3373, 3381.

In short, Ethicon’s request for judgment n.o.v. fails, as does its claim

that the trial court erred by declining to give a safer alternative design

instruction to the jury.

CAUSATION

Ethicon argues that Hammons failed to establish that a defect in Prolift

caused her injuries. We disagree.

Hammons introduced the causation testimony of Ralph Zipper, M.D., an

expert in urogynecology, including pelvic reconstructive surgery, vaginal

mesh, vaginal mesh procedures, and Prolift. Dr. Zipper reviewed Hammons’

medical history, the records of her treating physicians, and performed a

physical examination, all of which he described for the jury. N.T., 12/9/15

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J-A25032-17

(P.M.), at 24, 29-163. Dr. Zipper testified that Hammons presented to Dr.

Baker with anterior pelvic organ prolapse. At that time, he explained,

Hammons’ bladder bulged just beyond the opening of her vagina. She

experienced no pain, dyspareunia, or incontinence. She experienced these

symptoms several weeks after implantation. Dr. Zipper explained that

implantation with Prolift generated a chronic and progressive chain of

inflammation, scar plate formation, tissue contraction and erosion,

deformation of the vagina and pain. Dr. Zipper added that the mesh had

eroded through Hammons’ vaginal wall and adhered to the bladder, causing

her bladder to lose elasticity and creating urinary symptoms. Because of her

vaginal scars, Hammons lost elasticity and length in her vagina and

experienced severe dyspareunia and permanent sexual dysfunction. Id. at

29-32, 117-32.

Dr. Zipper excluded other potential causes of injury such as error by Dr.

Baker. He testified that Dr. Baker followed Ethicon-established protocol when

implanting the Prolift device and also performed optional procedures

recommended by Ethicon to increase the chances of success. He noted that

Dr. Heit’s examination of Hammons confirmed that Dr. Baker performed the

mesh implantation procedure correctly. Id. at 39-40, 97-104, 155.

Dr. Zipper testified that Hammons has a poor prognosis. Her injuries

continued after Dr. Heit removed part of the mesh, since part of the mesh

remains embedded in her bladder. She has tenderness near the top of her

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J-A25032-17

vagina and underneath her bladder and a recurrence of prolapse for multiple

organs. Her vagina is significantly foreshortened and has everted, or turned

inside out. She also lost bladder capacity and has bladder spasms. She

developed worsening of urgency and frequency of urination. Her dyspareunia

and sexual dysfunction has continued since her initial surgery in May 2009.

Id. at 134, 142-52.

Dr. Zipper opined that Hammons has few choices for further treatment

because there are no reasonable surgical or nonsurgical means to cure her

urinary and sexual dysfunction. Her pain and bladder-related complications

can be alleviated to some extent but not treated. Id. at 161-63.

Taken as a whole, this evidence sufficed to present the question of

causation to the jury. Although Ethicon contends that Dr. Zipper failed to

identify a specific defect of Prolift that caused her injuries, we find he testified

with the requisite degree of precision. He observed that the Prolift mesh

“degrades” and has a “tendency to cause prolapse in areas where you’re not

even operating.” N.T., 12/9/15 (P.M.), at 31. He added that the device “did

what we now know mesh and mesh with arms does. It contracted and it pulled

and it caused pain and it caused pain with intercourse that just didn’t go away.

And it also caused prolapse in other areas of her vagina.” Id. at 30. Pelvic

mesh, Dr. Zipper said, needs to be both soft and durable. N.T., 12/10/15, at

64. Prolift mesh, he stated, was not soft, id., and therefore caused injury.

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J-A25032-17

Ethicon argues that Dr. Zipper failed to rule out Dr. Baker’s surgical

technique as the cause of Hammons’ injuries. The evidence demonstrates

otherwise. Dr. Zipper testified that Dr. Baker attended Ethicon’s training and

performed Plaintiff’s Prolift implant as recommended by Ethicon by securing

the mesh to the apex of the vagina. Dr. Zipper also explained that Dr. Heit

found the mesh “bunched in the midline under the bladder neck and distal

bladder base,” and that this bunching demonstrated that the mesh was

defective rather than improperly placed. N.T., 12/9/15 (A.M.) at 40-41; 74,

98-102. Dr. Zipper concluded that “every bit of the medical record shows that

[Prolift] was put in correctly. It’s only years later that someone [Ethicon]

suggested it wasn’t.” N.T., 12/10/15 (P.M.), at 50. Ethicon points to

testimony by other physicians that mesh bunches only because of surgical

error, not defects in the mesh itself. Ethicon’s Opening Brief at 42. Once

again, Ethicon construes the evidence in the light most favorable to itself, the

incorrect standard at the judgment n.o.v. and appellate stages of review. The

jury was free to resolve conflicts between Hammons’ and Ethicon’s experts in

any way it saw fit. It chose to decide the issue in favor of Hammons. No

basis exists to disturb the jury’s determination.

EVIDENCE OF SPOLIATION

Ethicon seeks a new trial on the ground that the trial court improperly

admitted the deposition testimony of James Mittenthal, Ethicon’s corporate

designee, that Ethicon destroyed thousands of documents possessed by high-

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ranking Ethicon employees relating to the development of Prolift. Hammons

created the inference that Ethicon destroyed thousands of documents by

eliciting Mittenthal’s testimony that over 20,000 documents were in

computerized files of several Ethicon officials, while the computer hard drives

of other high-ranking officials were wiped clean. P-3411, at 744. Ethicon

admits that it destroyed multiple documents but claims that its conduct was

“inadvertent.” Ethicon’s Reply Brief at 26, 31. Notably, however, Ethicon

destroyed these documents even though counsel in pelvic mesh litigation had

issued notices directing Ethicon to preserve these documents. N.T., 12/3/15

(A.M.), at 16. The trial court permitted Mittenthal’s testimony but declined to

give an adverse inference instruction to the jury. Ethicon strenuously argues

that the admission of Mittenthal’s testimony prejudiced the jury.

The trial court gave the following reasons for permitting Mittenthal’s

testimony:

Despite preservation notices concerning pelvic mesh litigation,
thousands of documents were destroyed and could not be
produced to [Hammons]. Included in this destruction were
documents created by employees who were significantly involved
in the development, testing, and marketing of Prolift. The
custodial file of Dr. Owens, the world wide medical director of
[Ethicon’s] Women’s Health and Urology Program during the
development of Prolift, the individual responsible for managing
and improving premarket activities, had been destroyed. The
Court allowed [Hammons] to present evidence of the
unavailability of documentation and also allowed [Ethicon] to
present evidence concerning the reasons for the destruction,
which they claimed, was appropriate and inadvertent.

[Ethicon] contends that admission of Mr. Mittenthal’s deposition
testimony amounted to a sanction for spoliation. The decision to

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allow this evidence before the jury so that counsel could argue or
explain the failure to produce documents from these files at trial
is not a discovery sanction. [Hammons] specifically asked for an
adverse jury instruction. This was rejected by the court.

A jury is entitled to know what documentation was and was not
available to counsel in preparing and presenting their case. Given
this information the jury without any need for instruction from the
court could understand why other documents had not been
presented to them draw whatever conclusions were appropriate
from this evidence.

Trial Court Opinion, 9/30/16, at 17.

Ethicon argues that “without any factual or legal analysis of the issue,

the trial court simply allowed [Hammons] to present [Mittenthal’s testimony]

that spoliation occurred and left the jury to decide what to do with that

information.” Ethicon’s Opening Brief at 47. This decision, Ethicon continues,

was a misapplication of spoliation standards and a “sanction” against Ethicon.

The trial court knew this sanction was wrong, says Ethicon, given its

subsequent decision not to give an adverse inference instruction to the jury.

We do not agree.

Instead of admitting Mittenthal’s testimony without any analysis, the

court held a lengthy hearing outside the jury’s presence in which it admitted

certain passages of Mittenthal’s deposition testimony and excluded others.

N.T., 12/2/16 (A.M.), at 52-72. More importantly, the court was not required

to apply spoliation standards to this issue; nor did it do so. It applied the

correct analytical framework—principles of relevance and prejudice—and

acted within its discretion by admitting selected portions of Mittenthal’s

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testimony. Because the trial court did not utilize spoliations standards, its

ruling was not a spoliation sanction.

To explain why spoliation standards do not apply, we begin by describing

the spoliation doctrine:

As we observed in Rodriguez v. Kravco Simon Co., 111 A.3d
1191 (Pa. Super. 2015), penalties for spoliation of evidence have
been applied since the early 17th century. The spoliation doctrine
is applicable to any case “where ‘relevant evidence’ has been lost
or destroyed.” Mount Olivet Tabernacle Church v. Edwin L.
Wiegand Div., 781 A.2d 1263, 1269 (Pa. Super. 2001), aff’d
sub nom. Mount Olivet Tabernacle Church v. Edwin
Wiegand Div., 571 Pa. 60, 811 A.2d 565 (2002). A party’s
destruction or loss of proof that is pertinent to a lawsuit can result
in a variety of sanctions. Parr v. Ford Motor Co., 109 A.3d 682
(Pa. Super. 2014).

In reviewing the propriety of a sanction for spoliation, “we must
determine whether the court abused its discretion.” Id. at 701
(citation omitted). The trial court weighs three factors in deciding
upon an appropriate penalty for spoliation, “(1) the degree of fault
of the party who altered or destroyed the evidence; (2) the degree
of prejudice suffered by the opposing party; and (3) whether there
is a lesser sanction that will avoid substantial unfairness to the
opposing party and, where the offending party is seriously at fault,
will serve to deter such conduct by others in the future.” Id. at
702 (citation omitted). For purposes of

evaluation of the first prong, “the fault of the party
who altered or destroyed the evidence,” requires
consideration of two components, the extent of the
offending party’s duty or responsibility to preserve the
relevant evidence, and the presence or absence of bad
faith. The duty prong, in turn, is established where:
(1) the plaintiff knows that litigation against the
defendants is pending or likely; and (2) it is
foreseeable that discarding the evidence would be
prejudicial to the defendants.”

Id. (citations omitted).

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One sanction that a court may choose to impose when evidence
is lost or destroyed is to instruct the jury that it may infer “that
the destroyed evidence would have been unfavorable to the
position of the offending party.” Rodriguez, supra, at 1196. The
rationale for this spoliation inference is “nothing more than the
common sense observation that a party who has notice that
evidence is relevant to litigation and who proceeds to destroy
evidence is more likely to have been threatened by” the proof in
question. Id.

Gavin v. Loeffelbein, 161 A.3d 340, 353-54 (Pa. Super. 2017).

Sanctions for spoliation include, inter alia, entry of judgment against the

offending party, exclusion of evidence, monetary penalties such as fines and

attorney fees, and adverse inference instructions to the jury. Mt. Olivet

Tabernacle Church, 781 A.2d at 1272-73. The court decides whether to

impose sanctions by applying the three-prong test articulated in Gavin:

degree of fault, degree of prejudice and whether a lesser sanction is available.

Gavin, 161 A.3d at 353-54.

Spoliation standards do not apply, however, when the trial court merely

considers whether to permit evidence during trial that a party destroyed

documents. A decision cited in Ethicon’s brief, Caparotta v. Entergy Corp.,

168 F.3d 754 (5th Cir. 1990), is instructive.13 There, the district court declined

to give an adverse inference instruction to the jury but permitted the plaintiff

to introduce evidence that the defendant had destroyed documents. The Fifth

____________________________________________

13Decisions of lower federal courts may have persuasive, but not binding,
authority on this Court. Gongloff Contracting, L.L.C. v. L. Robert Kimball
& Assoc., Architects and Engineers, Inc., 119 A.3d 1070, 1078 n.6 (Pa.
Super. 2015).

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Circuit observed that the decision whether to give an adverse inference

instruction is distinct from the decision whether to admit evidence of

document destruction for the jury to consider with other trial evidence:

Entergy correctly points out that under this court’s holding in Vick
v. Texas Employment Commission, 514 F.2d 734, 737 (5th
Cir.1975), an adverse inference drawn from the destruction of
records is predicated on bad conduct by the defendant. Because
the district court found no bad faith, Entergy argues that evidence
of the inadvertent destruction of documents should not have been
presented to the jury.

Entergy is correct to the extent that it argues the spoliation
doctrine did not apply and that the jury could not be instructed
that the destroyed evidence was unfavorable to Entergy.
However, Vick does not apply to the issue of whether the district
court could nonetheless admit the fact of the destruction of
documents for the jury to weigh with the other evidence in the
case because such evidence was relevant.

Caparotta, 168 F.3d at 757. The proper test was not spoliation standards

but the usual evidentiary standards of relevance and prejudice. Id. at 757-

58.

Here, as in Caparotta, the trial court denied Hammons’ request for an

adverse inference instruction but permitted Hammons to introduce evidence

of Ethicon’s destruction of documents. Caparotta teaches that the test

governing admission of this evidence is relevance and prejudice, not the three-

prong spoliation test. As an appellate court, we review the trial court’s

application of relevance and prejudice standards for abuse of discretion.

Commonwealth v. Tyson, 119 A.3d 353, 357 (Pa. Super. 2015). “[A]n

abuse of discretion is not merely an error of judgment, but is rather the

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overriding or misapplication of the law, or the exercise of judgment that is

manifestly unreasonable, or the result of bias, prejudice, ill-will[,] or partiality,

as shown by the evidence or the record.” Commonwealth v. Cameron, 780

A.2d 688, 692 (Pa. Super. 2001).

We hold that the trial court acted within its discretion by permitting

Hammons to present Mittenthal’s testimony that Ethicon destroyed large

numbers of documents within the computer files of high-ranking Ethicon

officials. As the trial court observed in its opinion, Mittenthal testified that the

entire computerized files of multiple officers involved in Prolift’s development

were wiped away. P-3411, at 4, 16-19, 20-21. Since other high-ranking

officials at Ethicon had thousands of documents in their files, it was reasonable

to infer that the destroyed documents numbered in the thousands, if not in

the tens of thousands. The absence of these documents was relevant,

because Hammons had the burden of proof, and the jury might have held the

documents’ absence against her unless she demonstrated why they were

missing. Moreover, the absence of the documents was relevant to the jury’s

consideration of the credibility of witnesses whose documents were destroyed.

For example, Owens testified that she frequently communicated by email

about Prolift with Prolift’s inventors, Professor Jacquetin and Dr. Cosson. She

testified that Jacquetin and Cosson never indicated Prolift should not have

been launched in March 2005, or that Prolift was counter-indicated in sexually

active women. D-23 at 5-7. Because Ethicon wiped clean Owens’ custodial

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file, Hammons’ counsel was hampered in cross-examining Owens, because

counsel could not challenge her credibility on whether these purported

conversations took place or their content. Mittenhall’s testimony about

Ethicon’s destruction of records allowed Hammons to explain to the jury why

Owens’ email exchange was not presented for their consideration.

Not only was this evidence relevant, but it also was admissible under

Pa.R.E. 403, which provides: “The court may exclude relevant evidence if its

probative value is outweighed by a danger of one or more of the following:

unfair prejudice, confusing the issues, misleading the jury, undue delay,

wasting time, or needlessly presenting cumulative evidence.” “Unfair

prejudice” means “a tendency to suggest decision on an improper basis or to

divert the jury’s attention away from its duty of weighing the evidence

impartially.” Castellani v. Scranton Times, L.P., 124 A.3d 1229, 1245 (Pa.

2015) (citing Pa.R.E. 403 (Comment)). It is important to remember, however,

that

all relevant . . . evidence is meant to prejudice a defendant, [so]
exclusion is limited to evidence so prejudicial that it would inflame
the jury to make a decision based upon something other than the
legal propositions relevant to the case . . . [A] trial court is not
required to sanitize the trial to eliminate all unpleasant facts from
the jury’s consideration where those facts form part of the history
and natural development of the events . . .

Commonwealth v. Gonzalez, 112 A.3d 1232, 1238 n.6 (Pa. Super. 2015).

In other words, to paraphrase what our Supreme Court once said, a party may

strike hard blows so long as it does not strike foul blows. Commonwealth

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v. Cherry, 378 A.2d 800, 804 (Pa. 1977) (“while [a prosecutor] may strike

hard blows, he is not at liberty to strike foul ones”). The evidence of document

destruction in this case was highly relevant for the reasons provided in the

preceding paragraph. Its probative value outweighed any prejudice to

Ethicon. Indeed, we do not consider Ethicon to have suffered “unfair

prejudice,” Rule 403’s operative term.

Ethicon also argues that Hammons’ counsel made inflammatory and

prejudicial references to document destruction during closing argument.

Counsel stated:

And remember Mr. Mittenthal, and he was the fellow who told us
about the thousands of pages of documents that were destroyed
by Ethicon, these entire corporate files of high-ranking corporate
employees were wiped out. He told us that relevant documents
may have been destroyed, and to quote, “tens of thousands of
documents” were destroyed and it is possible that key documents
are missing. Now you know, I would rather believe that that
happened innocently, that it wasn’t done maliciously, that they
didn’t mean to destroy documents that things happen in
companies. Right?

N.T., 12/16/15 (PM) at 15-16. Several moments later, counsel added that

the loss of documents “tells you something about the corporate mindset,” and

“tells you a lot about their intentions.” Id. at 16

We do not consider this argument improper. A party is entitled to argue

the evidence during closing arguments, including all logical inferences.

Commonwealth v. Williams, 615 A.2d 716, 721-22 (Pa. 1992) (where

evidence of flight and concealment was introduced at trial, prosecutor was

entitled to remark during summation that evidence of flight is “relevant and

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admissible to establish an inference of guilt”); Hyrca v. West Penn

Allegheny Health Sys., 978 A.2d 961 (Pa. Super. 2009) (“[S]o long as no

liberties are taken with the evidence, a lawyer is free to draw such inferences

as he wishes from the testimony and to present his case in the light most

suited to advance his cause and win a verdict in the jury box”). Having

introduced evidence of document destruction during trial, counsel had the

right to present argument on this evidence in his closing argument along with

all logical inferences.

JURY INSTRUCTION RELATING TO HARM CAUSED BY PROLIFT

Ethicon objects to the jury instruction that “if Ethicon knew that a

surgeon using the product might place the Prolift incorrectly, then they’re

responsible for any harm which comes from the Prolift having been improperly

placed.” N.T., 12/18/15, at 35. Ethicon asserts that the trial court “essentially

instructed the jury to return a verdict for [Hammons] when it erroneously told

jurors that [Ethicon was] responsible for all misuse of Prolift.” Ethicon’s Brief

at 51. We disagree.

Our standard of review regarding jury instructions is limited to
determining whether the trial court committed a clear abuse of
discretion or error of law which controlled the outcome of the case.
Error in a charge occurs when the charge as a whole is inadequate
or not clear or has a tendency to mislead or confuse rather than
clarify a material issue. Conversely, a jury instruction will be
upheld if it accurately reflects the law and is sufficient to guide the
jury in its deliberations.

The proper test is not whether certain portions or isolated excerpts
taken out of context appear erroneous. We look to the charge in
its entirety, against the background of the evidence in the

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particular case, to determine whether or not error was committed
and whether that error was prejudicial to the complaining party.
In other words, there is no right to have any particular form of
instruction given; it is enough that the charge clearly and
accurately explains the relevant law.

Krepps v. Snyder, 112 A.3d 1246, 1256 (Pa. Super. 2015).

Here, the trial court gave the following pertinent instructions:

A product is defective if the seller fails to properly package or label
the product with reasonable warnings about the dangers of the
product or fails to give reasonably complete instructions about the
proper use of the product. A manufacturer has a duty to warn of
hidden dangers. If Ethicon knew that a surgeon using the
product might place the Prolift incorrectly, then they’re
responsible for any harm which comes from the Prolift
having been improperly placed.

****

A person’s conduct is legally responsible for causing an injury if
the injury would not have occurred without the conduct and the
injury was a natural, probable and foreseeable result of the
conduct. And that’s what we call responsible cause or cause in all
these questions that you’re going to have about cause. And there
can be more than one responsible cause of an injury. Now,
sometimes an unrelated event can break the connection between
a defendant’s negligent action and the injury. If this event was
not reasonably foreseeable, it is an intervening cause. When an
intervening cause breaks the connection between the defendant’s
negligent act and a plaintiff’s injury, a defendant’s negligent act is
no longer a responsible cause of that plaintiff’s injury.

N.T., 12/18/15, at 34-36 (emphasis added).

Quoting the bolded instruction in isolation, Ethicon argues that the trial

court wrongly instructed the jury to hold Ethicon liable for any physician

misuse. Under Indiana law, a medical device manufacturer has the duty to

warn treating physicians of the device’s “latent dangers.” Nat. Gas

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Odorking, 685 N.E.2d at 162. Device misuse is an intervening cause that

relieves the manufacturer of liability only if the misuse could not have been

reasonably foreseen by the manufacturer. Montgomery Ward & Co. v.

Gregg, 554 N.E.2d 1145, 1156 (Ind. App. 1990). The above instructions were

consistent with Indiana law and consistent with Indiana’s standard instruction

on the duty to warn.

Ethicon claims that this instruction amounted to a directive to reject

Ethicon’s argument that Hammons’ injuries were caused by Dr. Baker’s

surgical errors instead of any defect in Prolift. This is incorrect. The trial court

did not even mention Dr. Baker, let alone instruct the jury that his actions

were unrelated to Hammons’ injuries as a matter of law. Ethicon also made

arguments about Dr. Baker’s responsibility for Hammons’ injuries, which the

jury was free to accept or reject. N.T., 12/17/15 (A.M.), at 99. The trial court

made no instructional error.

AMOUNT OF COMPENSATORY DAMAGES

Ethicon argues that the trial court abused its discretion by denying

Ethicon’s post-trial motion for remittitur of the compensatory damage verdict

of $5.5 million. The trial court upheld the verdict based on Hammons’

“persistent pain and inability to have sex . . . the effect on her relationship

with her boyfriend, the effect on her self-image . . . the embarrassment and

humiliation she has suffered,” and her multiple surgeries. Trial Court Opinion,

9/30/16, at 21. We conclude that the trial court acted within its discretion.

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Our initial task is to determine whether Pennsylvania or Indiana law

applies to this issue. The parties do not appear to agree on this subject.

Hammons cites Pennsylvania cases in her brief, whereas Ethicon cites Indiana

cases. Because remittitur is a procedural mechanism under Pennsylvnaia law

rather than substantive law, the law of the forum state, i.e., Pennsylvania,

governs this issue.

“Procedural law is the set of rules which prescribe the steps by which

the parties may have their respective rights and duties judicially enforced[,]”

whereas “[s]ubstantive law is the portion of the law which creates the rights

and duties of the parties to a judicial proceeding.” Sheard v. J.J. DeLuca

Co., Inc., 92 A.3d 68, 76 (Pa. Super. 2014). “In conflicts cases involving

procedural matters, Pennsylvania will apply its own procedural laws when it is

serving as the forum state.” Commonwealth v. Sanchez, 716 A.2d 1221,

1223 (Pa. 1998). In contrast, where Pennsylvania substantive law conflicts

with another state’s law, Pennsylvania courts apply the law of the state which

has the most significant interest in the question. Murray v. Janssen

Pharmaceuticals, Inc., 180 A.3d 1235, 1252-53 (Pa. Super. 2018).

In Pennsylvania, remittitur is a procedural matter: it is the “procedural

[process] by which an excessive verdict of the jury is reduced.” Refuse

Management Systems, Inc. v. Consolidated Recycling and Transfer

Systems, Inc., 671 A.2d 1140, 1149 (Pa. Super. 1996). Accordingly, we

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apply Pennsylvania law to Ethicon’s challenge to the amount of compensatory

damages.14 Sanchez, 716 A.2d at 1223.

Under Pennsylvania law, the decision to grant a remittitur depends on

whether the award of compensatory damages lies beyond “the uncertain limits

of fair and reasonable compensation” or whether the verdict “so shocks the

conscience as to suggest that the jury was influenced by partiality, prejudice,

mistake, or corruption.” Potochnick v. Perry, 861 A.2d 277, 285 (Pa. Super.

2005). This standard is highly deferential, because the trial judge serves not

as finder of fact but as impartial courtroom authority with obligation to give

great respect to the jury’s function. Ferrer v. Trustees of Univ. of

Pennsylvania, 825 A.2d 591, 611 (Pa. 2002). If the compensatory award is

excessive, any remittitur must fix “the highest amount any jury could properly

____________________________________________

14 One distinction between the present case and Murray bears emphasis.
Murray was a products liability action against a pharmaceutical manufacturer
for failure to warn about the risks of a drug (risperidone). The plaintiff resided
in Maryland, was prescribed risperidone in Maryland and suffered harm from
the drug in Maryland. Following a verdict for the plaintiff, the trial court
reduced his compensatory damage award in accordance with Maryland’s
statutory cap on noneconomic damages. Both the trial court and the parties
referred to this reduction as a “remittitur.” Id., 180 A.3d at 1252. On appeal,
the plaintiff argued that the trial court erred in applying Maryland law because
remittitur is a procedural mechanism governed by Pennsylvania law. We
upheld the trial court’s decision on the ground that it did not actually exercise
a remittitur but correctly resolved a conflict of substantive law (Maryland’s cap
on damages versus Pennsylvania’s lack of any cap). In the present case,
Ethicon does not point to any pertinent substantive conflict between
Pennsylvania and Indiana damages law; nor are we aware of any. Instead,
Ethicon merely asked the trial court to perform a remittitur, a “procedural
mechanism” governed by Pennsylvania law. Id.

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award.” Neal v. Bavarian Motors, 882 A.2d 1022, 1028 (Pa. Super. 2005).

That amount “must necessarily be as high—and may well be higher—than the

level the court would have deemed appropriate if working on a clean slate.”

Id. This Court is not free to substitute its judgment for that of the fact finder.

“Rather, it is our task to determine whether the lower court committed a ‘clear’

or ‘gross’ abuse of discretion when conducting its initial evaluation of a

defendant’s request for remittitur.” Dubose v. Quinlan, 125 A.3d 1231,

1244 (Pa. Super. 2015) (citation omitted).

Each personal injury case “is unique and dependent on its own special

circumstances.” Kemp v. Philadelphia Transportation Co., 361 A.2d 362,

364 (Pa. Super. 1976). Thus, noneconomic loss must be measured by

experience rather than any mathematical formula. Martin v. Soblotney, 466

A.2d 1022, 1025 (Pa. 1983) (“it is immediately apparent that there is no

logical or experiential correlation between the monetary value of medical

services required to treat a given injury and the quantum of pain and suffering

endured as a result of that injury”). For this reason, the law entrusts jurors,

as the impartial acting voice of the community, to quantify noneconomic loss

and compensation. Nelson v. Airco Welders Supply, 107 A.3d 146, 161

(Pa. Super. 2014).

Hammons sought damages for all noneconomic losses recognized under

Indiana law, including pain and suffering; embarrassment and humiliation;

disfigurement; and loss of ability to enjoy the pleasures of life. See Ind. Model

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Civil Jury Instructions 703 (General elements of damages) and comments. To

determine damages within these categories of noneconomic loss, the jury is

entitled to consider the plaintiff’s age; the nature and extent of her injuries;

the effect of the injuries on her ability to function as a whole person; whether

the injuries are permanent; the physical pain and mental suffering she

experienced and will experience in the future as a result of the injuries; the

aggravation of a previous injury, disease, or condition; and the disfigurement

and/or deformity resulting from the injuries. Id.

Dr. Zipper examined Hammons and explained that she has tenderness

near the top of her vagina and underneath her bladder. Hammons’ prolapse

has recurred, implicating multiple organs. She has a significantly

foreshortened vagina, and her vagina has everted (turned inside out). She

testified her vagina is shortened and rigid with scar tissue because of Prolift

implantation and subsequent surgeries to remove mesh. Since May 2009, she

has suffered pain with sexual intercourse and has experienced incontinence.

She also continues to suffer pain when walking because mesh “arms” are

embedded in her muscles. These conditions are permanent. N.T., 12/9/15

(P.M.), at 32-33, 142-52, 161-63; N.T., 12/11/15 (P.M.), at 78-83, 136-38.

Dr. Zipper also described that Hammons has permanent loss of bladder

capacity and bladder spasms that cause a feeling of “urgency” and frequent

urination. These conditions also are permanent. Id. Hammons has

undergone three major surgeries but has no reasonable surgical or nonsurgical

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means of treatment to cure her urinary and sexual dysfunction. Her life

expectancy as of the time of trial was another 21.2 years. N.T., 12/9/15

(P.M.), at 32-33, 142-52, 161-63; N.T., 12/11/15 (P.M.), at 78-83, 136-38;

N.T., 12/18/15, at 40. Hammons testified her sexual dysfunction has affected

the relationship with her boyfriend of sixteen years, her self-image and her

happiness. She is embarrassed and humiliated by her physical deformity.

N.T., 12/9/15 (P.M.), at 32-33, 142-52. Collectively, this evidence

demonstrates Hammons suffered considerable physical disfigurement, pain,

suffering, embarrassment, and loss of life’s pleasures, and she will continue

to suffer these injuries for the remainder of her life. The court acted within

its discretion under these circumstances by determining that the verdict did

not shock its conscience.

Ethicon asks us to remit the verdict by comparing Hammons’s losses

with the plaintiffs’ injuries in Smalls v. Pittsburgh-Corning Corp., 843 A.2d

410 (Pa. Super. 2004), and Hartner v. Home Depot USA, Inc., 836 A.2d

924 (Pa. Super. 2003). In Smalls, an action against a manufacturer for

asbestos exposure, we remitted a $2 million verdict for pain and suffering

because the evidence demonstrated only that a sedentary, seventy-four-year-

old man with a twenty-year smoking habit and additional diseases unrelated

to asbestos exposure (cirrhosis, chronic obstruction pulmonary disease,

anemia, abdominal and colon conditions, and previously contracted

pneumonia) became winded after moderate exercise and no longer was as

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active around the house as he once was. Id., 843 A.2d at 417. In Hartner,

we remitted a $1 million verdict where the plaintiff sustained a knee injury

and undertook physical therapy but had no stiffness or swelling during

examination and used the gym three or four days a week. She did not seek

employer accommodations nor was there indication of necessity for ongoing

treatment. Id., 836 A.2d at 930. It is safe to say that Hammons has suffered,

and will continue to suffer for another two decades, far greater physical and

emotional trauma from Prolift than the plaintiff in Smalls suffered from

asbestos exposure or the plaintiff in Hartner suffered from her knee injury.

PUNITIVE DAMAGES

Prior to trial, the parties agreed that New Jersey law governed the issue

of punitive damages. The jury awarded Hammons $7 million in punitive

damages. Ethicon seeks judgment n.o.v. on the punitive damage verdict on

several grounds. We hold that the trial court properly denied judgment n.o.v.

New Jersey allows punitive damages if the plaintiff demonstrates that

the defendant acted with “wanton and willful disregard” of her rights and that

these acts caused her injuries. N.J. Stat. § 2A:15-5.12(a). Wanton and willful

disregard is “a deliberate act or omission with knowledge of a high degree of

probability of harm to another and reckless indifference to the consequences

of such act or omission.” N.J. Stat. § 2A:15-5.10. The standard of proof is

“clear and convincing evidence.” N.J. Stat. § 2A:15-5.12(a). The jury may

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consider all evidence relevant to the defendant’s misconduct and the plaintiff’s

injuries, such as:

(1) the likelihood, at the relevant time, that serious harm would
arise from the defendant’s conduct;

(2) the defendant’s awareness of reckless disregard of the
likelihood that the serious harm at issue would arise from the
defendant’s conduct;

(3) the conduct of the defendant upon learning that its initial
conduct would likely cause harm; and

(4) the duration of the conduct or any concealment of it by the
defendant.

N.J. Stat. § 2A:15-5.12(b). When a plaintiff complains that a defectively

designed medical device caused her injuries, the question of punitive damages

“may turn on whether the manufacturer wantonly disregarded a high

probability that injury would occur once the defect manifested itself in the

situation that the plaintiff encountered.” Zakrocki v. Ford Motor Co., 2009

WL 2243986 (N.J. Super. App. Div. July 29, 2009). When a plaintiff complains

that a failure to warn caused her injuries, punitive damages are appropriate

“where the manufacturer knew of the dangers created by its product and failed

to warn users of serious health hazards.” Gross v. Gynecare, 2016 WL

1192556, at *26 (N.J. Super. App. Div. 2016), certification denied, 2016 WL

7666693 (N.J. 2016).

In Gross, the New Jersey Appellate Division rejected Ethicon’s

arguments and affirmed a $7.76 million punitive verdict against Ethicon based

on evidence of its wanton and willful misconduct concerning Prolift. Hammons

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presented substantially the same evidence in this case. The evidence revealed

that Ethicon knew before launch that Prolift failed frequently and shortly after

implantation. Ethicon knew that nearly twenty percent of women would suffer

from mesh shrinkage that caused pain with sexual intercourse and

ambulation, and approximately twenty percent would suffer from mesh

erosion of surrounding vaginal tissue and other organs within one year of

implantation. Post-launch clinical data corroborated evidence that Prolift had

significant risks of injury and high rates of complications. N.T., 12/4/15

(P.M.), at 93-100; N.T. 12/7/2015 (A.M.) at 37-41; 48-50; N.T., 12/8/15

(A.M.), at 19-99; P -3402 at 3-52; P-3408 at 1-18.

Testimony also showed that Ethicon knew that women would require

additional surgeries to correct mesh injuries. By 2006, Ethicon documents

revealed that the company knew women who turned “to surgery to deal with

a bad Prolift” would be a “disaster.” And Ethicon knew human tissue continues

to react to mesh for decades because it is designed as a permanent implant.

Yet Ethicon failed to study any long-term consequences or to develop any

process to remove Prolift from women who suffered complications. Id.

Ethicon recognized Prolift’s risks but nevertheless continued to sell the product

without adequate warnings. The issues were so serious that Prolift’s inventors

and designers, Professor Jacquetin and Dr. Cosson, expressed their concerns

about the mesh to Ethicon and repeatedly urged Ethicon to replace Prolene

soft/Gynemesh with Ultrapro, an existing, safer mesh product. Nevertheless,

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the Prolift+M (with Ultrapro) project went into “limbo” because it would have

delayed launch and affected Prolift’s profitability. By 2008, two-thirds of

surgeons who implanted Prolift were reluctant to use the device in sexually

active patients. Physicians asked Ethicon for a mesh that was lighter, softer

and caused fewer erosions and less pain, but Ethicon continued to sell the

product as designed and without adequate warnings. Id.

Ethicon also sold the product and failed to disclose known information

to treating physicians about the severity, incidence, and permanence of

complications. Before launch, Ethicon rebuffed its scientific director, Dr.

Arnaud, who proposed disclosures in the IFU that would have properly warned

that: (1) mesh erosion and retraction of the Prolift mesh could result in

“anatomic distortion” of the vaginal cavity that would “interfere with sexual

intercourse,” and (2) this risk should be “taken in consideration when the

procedure is planned in a sexually active woman.” Ethicon refused to include

this warning because Prolift’s IFU had already been printed for launch. Later

printings also failed to include the warning. Id.

At the same time, Ethicon actively misrepresented Prolift’s essential

properties in the Prolift IFU. Ethicon’s employees acknowledged Prolift’s IFU

description was “unsupportable” and lacked foundation in clinical data. They

said that the IFU’s characterization of Prolene/Gynemesh as “soft” was an

“illusion.” They also said the claim of “bi-directional elastic property” that

“allows adaption to various stresses encountered by the body” had no support

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in data. Ethicon had pulled a mesh “out of our existing bag of tricks” for

Prolift. P-3401 at 3; P-3416 at 6-7. Ethicon’s medical director described the

mesh as “the best of a bad lot.” P-3415 at 5. Such evidence permitted the

jury to find Ethicon acted with wanton and willful disregard of Hammons’

rights. N.J. Stat. § 2A:15-5.10 & 2A:15-5.12.

Ethicon contends punitive damages are unavailable under New Jersey

law because the parties stipulated that Prolift was “properly and lawfully

marketed.” Ethicon’s Brief at 57. The New Jersey Products Liability Act

(“NJPLA”) provides a defense to punitive damages for a manufacturer whose

medical device “was approved or licensed; or is generally recognized as safe

and effective” by the Food and Drug Administration. N.J. Stat. § 2A:58C-5c

(“FDA punitive damage exemption”). Ethicon’s brief, however, completely

fails to analyze whether the stipulation that Prolift is “properly and lawfully

marketed” satisfies the FDA punitive damage exemption. The only decision

Ethicon cites, Pavlova v. Mint Mgt. Corp., 868 A.2d 322, 328 (N.J.App.Div.

2005), does not analyze the FDA punitive damage exemption at all. Thus,

this argument fails.15

____________________________________________

15 From other decisions involving Ethicon, it appears that the path that Prolift
took to reach the market does not satisfy the FDA punitive damage exemption.
Ethicon apparently went through the FDA's 510(k) clearance process, in which
the FDA permits marketing of a product if it concludes that the device is
‘substantially equivalent’ to a pre-existing, previously approved device.
Lewis v. Johnson & Johnson, 991 F. Supp. 2d 748, 751-52 (S.D.W.Va.
2014) (pelvic mesh decision). Lewis held, after exhaustive analysis, that

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Ethicon also argues that Prolift’s IFU warned of the “majority of risks”

relevant to Hammons’ injuries. Ethicon’s Brief at 59. In so many words, Prolift

argues that some labeling is sufficient to avoid punitive damages, even if the

labeling is incomplete. Perhaps this argument would have force if the

omissions from labeling are unimportant, but the omissions in this case clearly

were material. Here, however, Ethicon’s IFU, sales brochures, and other

physician communications omitted crucial warnings of severe complications

experienced by Hammons, so much so that the jury could find punitive liability

against Ethicon. See In re C.R. Bard, Inc., 2013 WL 2432871, at *7 (S.D.

W. Va. June 4, 2013) (“the fact that [defendant] provided warnings regarding

certain issues is simply not dispositive” as to punitive damages liability);

Thom v. Bristol-Myers Squibb Co., 353 F.3d 848, 853 (10th Cir. 2003)

(same).

DELAY DAMAGES

In her cross-appeal, Hammons argues that the trial court should have

awarded delay damages on the punitive damage portion of the verdict instead

of on the compensatory portion only. We disagree.

Pa.R.Civ.P. 238 governs the application of delay damages. In 1983, our

Supreme Court held in Colodonato v. Consolidated Rail Corp., 470 A.2d

475 (Pa. 1983), that Rule 238 limits the calculation of delay damages to

____________________________________________

510(k) clearance of Ethicon’s pelvic mesh products did not constitute a finding
by the FDA that the products were safe or effective. Id. at 751-56.

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compensatory damages. Hammons contends that Colodonato no longer

controls due to an amendment to Rule 238 in 1988. We do not find the

amendment expands Rule 238’s reach to punitive damages.

The 1979 version of Rule 238, which was in effect at the time the

Supreme Court decided Colodonato, provided in relevant part:

(a) Except as provided in subdivision (e), in an action seeking
monetary relief for bodily injury, death or property damage, or
any combination thereof, the court or the arbitrators appointed
under the Arbitration Act of June 16, 1836, P.L. 715, as amended,
5 P.S. § 30 et seq., or the Health Care Services Malpractice Act of
October 15, 1975, P.L. 390, 40 P.S. § 1301.101 et seq., shall

(1) add to the amount of compensatory damages in the award of
the arbitrators, in the verdict of a jury, or in the court’s decision
in a nonjury trial, damages for delay at ten (10) percent per
annum, not compounded, which shall become part of the award,
verdict or decision . . . .

In 1986, the Supreme Court held in Craig v. Magee Memorial

Rehabilitation Center, 515 A.2d 1350 (Pa. 1986), that former Rule 238 was

unconstitutional because it created an uncontestable presumption that all fault

in the time it takes to proceed to trial lies with the defendant. The 1988

amendments resolved that issue by excluding the time during which the

plaintiff caused a delay of the trial. Conner v. Munsey, 620 A.2d 1103, 1104

(Pa. 1993).

Under the 1988 amendments, Rule 238 provided in relevant part:

(a)(1) At the request of the plaintiff in a civil action seeking
monetary relief for bodily injury, death or property damage,
damages for delay shall be added to the amount of
compensatory damages awarded against each defendant or
additional defendant found to be liable to the plaintiff in the verdict

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of a jury, in the decision of the court in a nonjury trial or in the
award of arbitrators appointed under section 7361 of the Judicial
Code, 42 Pa.C.S. § 7361, and shall become part of the verdict,
decision or award.

(2) Damages for delay shall be awarded for the period of time
from a date one year after the date original process was first
served in the action up to the date of the award, verdict or
decision.

(3) Damages for delay shall be calculated at the rate equal to the
prime rate as listed in the first edition of the Wall Street Journal
published for each calendar year for which the damages are
awarded, plus one percent, not compounded.

(b)(1) The period of time for which damages for delay shall be
calculated under subdivision (a)(2) shall exclude the period of
time, if any,

(i) after the defendant made a written offer which complied with
the requirements of subdivision (b)(2), provided that the plaintiff
obtained a recovery which did not exceed the amount described
in subdivision (b)(3), or

(ii) during which the plaintiff caused delay of the trial.

[Emphasis added]. Amended Rule 238(b) keyed the time frame for the

calculation of damages to a new (a)(2), with deductions of any of the time

found under (b)(1)(i) or (ii).

The rule was restructured slightly for the amended rule to make sense.

In both versions, the provision for delay damages identified: (1) the actions

to which it applies; (2) limited its application to compensatory damages; (3)

the rate; and (4) the time to be used in computing delay damages. There is

nothing about the amendment, the explanation provided by the Civil

Procedural Rules Committee, or the case law construing the rule that suggests

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the Supreme Court meant “compensatory damages” in 1988 to mean anything

other than what it meant in 1979. The language that was critical to the

Supreme Court’s holding in Colodonato remained unchanged. Id., 470 A.2d

at 477 (“The language of section (a)(1) of the rule makes it clear that the

delay damage provision therein specifically relates to that portion of an award,

verdict, or decision . . . which comprises compensatory damages”).

Following the 1988 amendments, this Court has cited Colodonato in

construing the scope of delay damages as limited. See Hodges v.

Rodriguez, 645 A.2d 1340, 1349-50 (Pa. Super. 1994) (citing Colodonato

for the proposition that delay damages are inapplicable to punitive damages).

Hammons does not cite any post-amendment decisions that hold or suggest

that Rule 238 applies to punitive damages. To the contrary, both the Supreme

Court and this Court have consistently “emphasized the narrow breadth of the

Rule.” Touloumes v. E.S.C., Inc., 899 A.2d 343, 348-49 (Pa. 2006); see

also Anchorstar, Jr. v. Mack Trucks, Inc., 620 A.2d 1120, 1121 (Pa. 1993)

(refusing to extend delay damages to loss of consortium claims); Musumeci

v. Penn’s Landing Corp., 640 A.2d 416, 420-22 (Pa. Super. 1994) (no delay

damages for personal injury claim governed by federal maritime law);

Thompson v. T.J. Whipple Constr. Co., 985 A.2d 221, 230 (Pa. Super.

2009) (delay damages not recoverable when terms of high-low agreement

would be contravened); Wagner v. Orie & Zivic, 636 A.2d 679, 681 (Pa.

Super. 1994) (refusing to extend delay damages to legal malpractice with

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regard to personal injury claim based on pre-amendment Supreme Court

holding).

For these reasons, we hold that the 1988 amendments to Rule 238 did

not make delay damages applicable to an award of punitive damages.

Judgment affirmed. Ethicon’s application to strike supplemental trial

court record denied. Hammons’s application for post–submission

communication to report about developments in the trial court concerning

orders under appeal denied.

Judgment Entered.

Joseph D. Seletyn, Esq.
Prothonotary

Date: 6/19/18

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