Teresa Taylor v. Mentor Worldwide, LLC

940 F.3d 582
CourtCourt of Appeals for the Eleventh Circuit
DecidedOctober 8, 2019
Docket16-17147
StatusPublished
Cited by43 cases

This text of 940 F.3d 582 (Teresa Taylor v. Mentor Worldwide, LLC) is published on Counsel Stack Legal Research, covering Court of Appeals for the Eleventh Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Teresa Taylor v. Mentor Worldwide, LLC, 940 F.3d 582 (11th Cir. 2019).

Opinion

Case: 16-17147 Date Filed: 10/08/2019 Page: 1 of 69

[PUBLISH]

IN THE UNITED STATES COURT OF APPEALS

FOR THE ELEVENTH CIRCUIT ________________________

No. 16-17147 ________________________

D.C. Docket Nos. 4:08-md-02004-CDL, 4:12-cv-00176-CDL

TERESA TAYLOR,

Plaintiff – Appellee,

versus

MENTOR WORLDWIDE LLC, MENTOR CORPORATION,

Defendants – Appellants.

________________________

No. 16-17245 ________________________

D.C. Docket Nos. 4:08-md-02004-CDL 4:12-cv-00176-CDL

In re: MENTOR CORP. OBTAPE TRANSOBTURATOR SLING PRODUCTS LIABILITY LITIGATION. __________________________________________________________________ Case: 16-17147 Date Filed: 10/08/2019 Page: 2 of 69

Plaintiff – Appellant,

Defendants – Appellees.

Appeals from the United States District Court for the Middle District of Georgia ________________________

(October 8, 2019)

Before TJOFLAT and JULIE CARNES, Circuit Judges, and KAPLAN,∗ District Judge.

KAPLAN, District Judge:

Teresa Taylor here sues Mentor Worldwide LLC (“Mentor”) and Mentor

Corporation 1 for compensatory and punitive damages for injuries she suffered as a

result of the surgical implantation of a polypropylene mesh sling manufactured by

Mentor to treat her stress urinary incontinence. The jury found Mentor liable to

Taylor for failure to warn both before and after implantation, defective design, and

negligence. It awarded $400,000 in compensatory and $4 million in punitive

∗ The Honorable Lewis A. Kaplan, of the United States District Court for the Southern District of New York, sitting by designation. 1 Mentor Corporation merged into Mentor Worldwide LLC and consequently ceased to exist prior to the filing of the complaint.

2 Case: 16-17147 Date Filed: 10/08/2019 Page: 3 of 69

damages. Mentor moved for judgment as a matter of law or, in the alternative, for a

new trial or to reduce the punitive damages award. The district court upheld the

jury’s verdict with respect to liability and compensatory damages, but concluded that

the punitive damages award exceeded Florida’s statutory cap and consequently

reduced the punitive damages award to $2 million.

Mentor now appeals. It contends that it is entitled to judgment as a matter of

law because the district court erred in (1) receiving certain expert testimony on the

issue of specific causation and (2) applying an incorrect causation standard to

Taylor’s failure to warn claims. Mentor argues, in the alternative, that it is entitled

to a new trial on the basis of various evidentiary rulings by the district court or to an

amended judgment eliminating or further reducing the punitive damages award.

Taylor cross appeals, arguing that the district court erred in reducing the punitive

damages awarded by the jury. We find no error in the judgment and therefore affirm.

I. BACKGROUND

This is one of more than 800 cases that were consolidated by the Judicial Panel

on Multidistrict Litigation into the multidistrict proceeding known as In re Mentor

Corp. ObTape Transobturator Sling Products Liability Litigation, No. 4:08-MD-

2004 (CDL). The cases arise from claims of medical complications allegedly

associated with a polypropylene mesh sling manufactured by Mentor called ObTape.

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One such case, brought by Taylor, who was surgically implanted with ObTape in

2004 to treat stress urinary incontinence, was selected to go to trial as a bellwether.

Taylor claimed defective design, negligence, and failure to warn both before

and after implantation of the ObTape. She contended that her ObTape implant

caused her to suffer from a thinning of her urethral wall and from chronic bladder

inflammation (also called cystitis). At trial, she endeavored to prove that her injuries

resulted from two design defects in the ObTape, namely, a small pore size, which

allegedly did not allow adequate tissue ingrowth, and an alleged propensity to

degrade and shed polypropylene particles in the body. She relied at trial on several

expert witnesses to establish both general causation – that is, that ObTape was

capable of causing the types of injuries from which she suffered – and specific

causation – that is, that the ObTape implanted in her in fact caused her injuries.

We begin with an overview of the evidence offered and objections made at

trial to the extent such evidence and objections are relevant on appeal.

A. General Causation

1. Porosity of ObTape

Several witnesses testified, in their respective expert opinions, that ObTape’s

small pore size did not allow adequate tissue ingrowth, which in turn led to

inflammation, erosion, and infection.

4 Case: 16-17147 Date Filed: 10/08/2019 Page: 5 of 69

One such witness was Dr. William Hyman, a professor emeritus of biomedical

engineering at Texas A&M University. Dr. Hyman testified that large pores are

better than small pores in a mesh sling implant such as ObTape. He explained that

the goal is for the tissue to grow into the implant and to “stabilize it and hold it in

place” in order to prevent the implant from “moving relative to the tissue.”

According to Dr. Hyman, if an implant has “big holes and relatively little material,”

the “[t]issue can grow through the holes, find other tissue on the other side, and

anchor it all in place, and that helps control erosion.”2 He testified also about the

ObTape sling in particular and opined that it had a “uniquely bad” design in part

because it had a small pore size as well as smaller numbers of pores. In other words,

according to Dr. Hyman, the small pore size of ObTape prevented adequate tissue

ingrowth, which then permitted the ObTape to move around the implant area and

cause erosion.3

Dr. Andrew Siegel, a urologist, testified along similar lines, saying that, in his

experience with his patients, ObTape “didn’t develop the typical tissue ingrowth and

incorporation that [he] had come to expect with some of the previous generation

2 Dr. Hyman explained that erosion occurred when tissue was “essentially . . . rubbed through by [a] foreign object.” 3 He explained also that the small pores in ObTape trapped bacteria and prevented the body from fighting infection.

5 Case: 16-17147 Date Filed: 10/08/2019 Page: 6 of 69

sling materials” and that the implant’s pores were not big enough to allow adequate

tissue ingrowth.

2. Tendency to Degrade

Dr. Ahmed El-Ghannam, a professor of biomaterials at the University of

North Carolina, testified on the degradation theory. He said that he had conducted

a series of scientific experiments on ObTape, including an electron microscope

examination of the product after immersing it in a physiological solution, a Fourier

Transform Infrared Spectroscopy, a gas chromatography/mass spectrometry

analysis of a physiological solution after the ObTape had been immersed in it, a

differential scanning calorimetry, and an x-ray diffraction analysis. Each analysis,

he said, confirmed that ObTape, although intended to be an inert, permanent

material, had a propensity to degrade and shed polypropylene particles in the body.

He testified that this degradation and shedding of particles sparked a reaction by the

body’s immune system, causing the body continuously to release hydrogen peroxide

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