Patricia Perryman v. Mentor Worldwide LLC

CourtCourt of Appeals for the Eleventh Circuit
DecidedAugust 28, 2018
Docket16-16645
StatusUnpublished

This text of Patricia Perryman v. Mentor Worldwide LLC (Patricia Perryman 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
Patricia Perryman v. Mentor Worldwide LLC, (11th Cir. 2018).

Opinion

Case: 16-16645 Date Filed: 08/28/2018 Page: 1 of 12

[DO NOT PUBLISH]

IN THE UNITED STATES COURT OF APPEALS

FOR THE ELEVENTH CIRCUIT ________________________

No. 16-16645 ________________________

D.C. Docket Nos. 4:08-md-02004-CDL; 4:13-cv-00400-CDL

In re: Mentor Corp. Obtape Transobturator Sling Products Liability Litigation.

__________________________________________________________________

PATRICIA PERRYMAN,

Plaintiff - Appellant,

versus

MENTOR WORLDWIDE LLC,

Defendant - Appellee.

________________________

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

(August 28, 2018) Case: 16-16645 Date Filed: 08/28/2018 Page: 2 of 12

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

JULIE CARNES, Circuit Judge:

To treat the stress urinary incontinence of plaintiff Patricia Perryman

(“Plaintiff”), her doctor surgically implanted one of Mentor Worldwide LLC’s

ObTape vaginal mesh products. Post-surgery, Plaintiff experienced a number of

symptoms, including pain, tenderness, and infections, all of which were known

side effects of mesh implants. Notwithstanding repeated visits to her doctor, as

well as excisions of mesh that had begun protruding, Plaintiff’s symptoms

persisted. As a result, she eventually had the ObTape replaced with a different

product, and her symptoms largely went away.

Seven years later, after learning from a television commercial that her post-

operative symptoms may have been caused by defects in the ObTape, Plaintiff

filed this products liability suit against Mentor in federal court. Mentor filed a

motion for summary judgment arguing that Plaintiff’s lawsuit was time-barred

because her claim accrued by the time her ObTape implant was removed, yet

Plaintiff did not file suit until seven years later—well outside the four-year statute

of limitations period provided for by applicable Florida law. The district court

* Honorable Lewis A. Kaplan, Senior United States District Judge for the Southern District of New York, sitting by designation.

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agreed, holding that, because Plaintiff was aware that her symptoms were related

to the implantation of the ObTape mesh by the time it was removed, her claim

accrued at that time and her subsequent lawsuit was several years too late.

Since the district court’s ruling, however, our court has addressed this very

same statute of limitations question under Florida law. See Eghnayem v. Boston

Sci. Corp., 873 F.3d 1304 (11th Cir. 2017). We must apply the standard used in

Eghnayem for review of this particular question and, upon doing so, we conclude

that a question of fact exists as to Mentor’s defense and therefore reverse the

district court’s grant of summary judgment to Mentor.

I. BACKGROUND

A. Factual Background

In May 2005, Plaintiff’s doctor surgically implanted a Mentor ObTape

vaginal mesh “sling” to treat Plaintiff’s stress urinary incontinence. Before the

surgery, Plaintiff’s doctor explained that the surgery had inherent risks, including

bleeding, infection, urinary retention, injury to tissue, and pelvic pain. Likewise,

mesh products themselves pose inherent risks. Plaintiff was informed that even if

the mesh was properly implanted and even if there was nothing wrong with it, her

body could nonetheless reject the product, and the mesh could protrude through the

vaginal wall or cause infection. Indeed, Mentor’s Product Insert Data Sheet

3 Case: 16-16645 Date Filed: 08/28/2018 Page: 4 of 12

(essentially an informational pamphlet for doctors) indicated that “[v]aginal

erosion, urethral evocation, and infection” were possible ObTape side effects,

though they were reported “very rarely.”

Plaintiff’s surgery itself was unremarkable, but its consequences had a

lasting impact. The surgery resolved her incontinence, but Plaintiff began

experiencing vaginal infections along with pain and discomfort in her pelvic

region. Over the course of roughly six months, Plaintiff repeatedly met with her

doctor and complained of urinary retention, infections and the resulting vaginal

discharge, and pain and tenderness during intercourse.

On multiple occasions, her doctor inspected her vagina, observed protruding

mesh, and excised it. Despite the excisions, Plaintiff’s symptoms persisted.

Eventually, in February 2006, Plaintiff decided to switch doctors. Her new doctors

recommended removal of the ObTape.

Accordingly, on February 17, Plaintiff’s new doctors surgically removed her

ObTape and replaced it with a different sling. The new sling was a “natural

product” made with biological material that may be more likely to integrate with

the human body than plastic synthetics like ObTape. During the surgery, one

doctor definitively concluded that Plaintiff’s ObTape had eroded through her

vaginal tissue.

4 Case: 16-16645 Date Filed: 08/28/2018 Page: 5 of 12

Plaintiff experienced no complications from her replacement surgery.

Moreover, the infections and discharge stopped. Plaintiff believed that this

positive outcome was the result of her body accepting the new mesh material better

than it had accepted the ObTape material. Nonetheless, some portions of

Plaintiff’s ObTape sling could not be removed. As a result, Plaintiff continues to

experience some tenderness and pain.

After her initial surgery in May 2005, Plaintiff never felt that her ObTape

implant was functioning properly. She reached this conclusion because, before

receiving the implant, she had never experienced the symptoms of discomfort,

pain, vaginal discharge, and infections that occurred after the surgery. When

Plaintiff began experiencing these symptoms post-surgery, she “didn’t know what

caused” them and thought she “was just having an allergy to” the ObTape implant

or her body was “rejecting . . . it or something.” As to why her ObTape implant

was continually protruding, she thought this was because either her “body just

wasn’t accept[ing] it or maybe . . . [she] had an infection that was keeping things

not healing right.” Altogether, Plaintiff “thought the problems were related to

[her] personally or perhaps caused by some other factor besides the mesh.”

Plaintiff never suspected that ObTape was defective or that a specific defect in her

5 Case: 16-16645 Date Filed: 08/28/2018 Page: 6 of 12

ObTape implant had caused her injuries until she saw a commercial in 2013 that

reported the existence of vaginal sling defects.

B. Procedural History

Alerted by television commercials to the fact that her symptoms may have

been caused by defects in the ObTape, on September 4, 2013, Plaintiff filed a

lawsuit in federal court as part of a consolidated multidistrict litigation action

against Mentor over ObTape’s alleged defects. 1 See In re: Mentor Corp. ObTape

Transobturator Sling Prods. Liab. Litig., 588 F. Supp. 2d 1374 (J.P.M.L. 2008).

Plaintiff alleged claims based on products liability, including negligence,

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In Re Mentor Corp. Obtape Transobturator Sling Products Liability Litigation
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Patricia Perryman v. Mentor Worldwide LLC, Counsel Stack Legal Research, https://law.counselstack.com/opinion/patricia-perryman-v-mentor-worldwide-llc-ca11-2018.