Corder v. Ethicon, Inc.

CourtDistrict Court, E.D. Kentucky
DecidedJuly 21, 2020
Docket6:19-cv-00273
StatusUnknown

This text of Corder v. Ethicon, Inc. (Corder v. Ethicon, Inc.) is published on Counsel Stack Legal Research, covering District Court, E.D. Kentucky primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Corder v. Ethicon, Inc., (E.D. Ky. 2020).

Opinion

UNITED STATES DISTRICT COURT EASTERN DISTRICT OF KENTUCKY SOUTHERN DIVISION LONDON

VIRGINIA CORDER, ) ) Plaintiff,1 ) ) No. 6:19-CV-273-REW v. ) ) ETHICON, INC., et al., ) OPINION & ORDER ) Defendants. ) )

*** *** *** *** A little more than 13 years ago, a gynecologist told a struggling Virginia Corder that choosing Ethicon’s pelvic mesh products would be “the best thing that would ever happen” to her. Corder took that advice and signed on for surgical implantation of two Ethicon devices. Per Corder, what followed were years of debilitating complications and removal surgery. Corder blames Ethicon and filed this suit to prove recover for her harms. I. BACKGROUND Defendant Ethicon, Inc., a Johnson & Johnson subsidiary,2 manufactured, marketed, and sold pelvic mesh products aimed primarily at the treatment of female pelvic organ prolapse and stress urinary incontinence. In 2007, Plaintiff Virginia Corder, suffering from cystocele3 and

1 Because Defendants’ motion does not challenge consortium-Plaintiff Larry Corder’s lone claim, this ruling concerns only Virginia Corder. 2 The Court refers to the defense, Ethicon however named and Johnson & Johnson, collectively as “Defendants” or “Ethicon.” 3 Per the Cleveland Clinic, “a prolapsed, herniated, dropped or fallen bladder[.]” Cystocele, https://my.clevelandclinic.org/health/diseases/15468-cystocele-fallen-bladder (last visited July 7, 2020). Plaintiff’s response brief also alleges that Corder suffered from “stress urinary incontinence[.]” DE 54 at 1. However, the documents Corder submitted in conjunction with her urinary retention, consulted with her gynecologist, Dr. Kimberly Bush, regarding treatment options. See DE 5 at 6 (Pl.’s Fact Sheet).4 Corder, herself a registered nurse, inquired about an “old fashioned” bladder tack procedure—involving use of the patient’s own tissue to surgically “tack up” (via sutures) the prolapsed bladder. Corder Dep. at 142–43. However, Dr. Bush advised that Ethicon’s Prolift+M and TVT-SECUR implants were the better solution. Indeed, Bush confidently

predicted that implanting Ethicon’s devices would be “the best thing that would ever happen to” Corder. Id. After reviewing an Ethicon pamphlet (supplied by Dr. Bush), and “trust[ing]” her gynecologist’s recommendation, id., Corder chose to go with Defendants’ products. Dr. Bush surgically implanted the devices on March 30, 2007. DE 52-1 at 3. Unfortunately, the mesh implants did not, as Corder tells it, prove the boon that Bush forecasted. Per Plaintiff, the implants’ effects were numerous and uniformly negative. Among other complications, Corder claims: pain in multiple areas (abdomen, low back, hip), incontinence (urinary and bowel), loss of sensation, abscesses, bleeding, inability to have (or pain during) intercourse, urinary tract infections, cloudy vision, bloody discharge, and bladder spasms. DE 5 at

7; Corder Dep. at 66–67. Plaintiff claims these symptoms began appearing “directly after” her surgery and that they persisted, at least in part, through her claim date, nearly a decade post-op. DE 5 at 8. Dr. Bush advised Corder that her post-surgery symptoms “were normal[.]” Id. However, Corder “suspected” that the implants were the cause of her maladies. And, a 2016 examination (by

originating MDL pleading appear to reject a pre-surgical incontinence diagnosis. See DE 5 at 6; DE 6 at 1. 4 Though the docketed fact sheet does not include an attached verification, the subsequent entry includes as its final page a sworn declaration of veracity concerning “the final copy of this Plaintiff Fact Sheet[.]” DE 6 at 6. Given document pagination, (and the preceding verification concerning the DE 6 “Plaintiff Profile Form,” id. at 5) the Court reasonably infers that Corder verified the fact sheet and that the attachment was misfiled or mis-docketed. Ethicon makes no issue of this. Dr. Donna Nall) revealed “a wad of mesh and erosion” that confirmed Plaintiff’s suspicions. Id. at 8, 13. The examining physician referred Corder to Dr. Rudolph Tovar for a June 3, 2016, removal operation. Id. at 8, 12. Dr. Tovar was able to remove only parts of the mesh because, per Plaintiff, portions were inextricably fused with Corder’s “tendons and pelvic region.” Id. at 7. Plaintiff, seeking to hold Ethicon liable under various theories, filed suit on November 16,

2016. See DE 1 (Short Form Complaint). Corder joined hundreds of other Ethicon-product plaintiffs in a Southern District of West Virginia hosted MDL. Following initial processing, the MDL Court transferred this matter to this District for final resolution. See DE 40 (Transfer Order). Ethicon’s motion for partial summary judgment now pends. DE 52. Plaintiff brings 18 claims. See DE 1 at 4–5 (asserting Counts I–XVIII of the operative master complaint); DE 42-1 (Am. Master Compl.). Defendants’ motion challenges eleven of Corder’s theories, including: strict liability based on failure to warn, manufacturing and/or product defects (Counts II–IV, DE 42-1 ¶¶ 95–114), fraud (Count VI, id. ¶¶ 119–47), fraudulent concealment (Count VII, id. ¶¶ 148–56), constructive fraud (Count VIII, id. ¶¶ 157–64), negligent misrepresentation (Count IX, id. ¶¶ 165–

69), express and implied warranty breaches (Count XI & XII, id. ¶¶ 174–96), violation of consumer protection laws (Count XIII, id. ¶¶ 197–215), and unjust enrichment (Count XV, id. ¶¶ 221–25). The motion—fully briefed, see DE 54 (Resp.), DE 55 (Reply)5—stands ripe for review. For the following reasons, and under the applicable standards, the Court finds Defendants’ requests only partly warranted. Plaintiff abandons one claim (Count II), another is unnecessarily redundant (Count IV), and three others (Counts XI–XIII) are fatally flawed. The balance of the claim slate survives Ethicon’s Rule 56 challenge on the terms here stated.

5 Plus, supplemental authority filings. See DE 56, 64, 66 & 68. II. APPLICABLE STANDARDS A court “shall grant summary judgment if the movant shows that there is no genuine dispute as to any material fact and the movant is entitled to judgment as a matter of law.” Fed. R. Civ. P. 56(a). A reviewing court must construe the evidence and draw all reasonable inferences from the underlying facts in favor of the nonmoving party. Matsushita Elec. Co., Ltd. v. Zenith

Radio Corp., 106 S. Ct. 1348, 1356 (1986); Lindsay v. Yates, 578 F.3d 407, 414 (6th Cir. 2009). Additionally, the court may not “weigh the evidence and determine the truth of the matter” at the summary judgment stage. Anderson v. Liberty Lobby, Inc., 106 S. Ct. 2505, 2511 (1986). The burden of establishing the absence of a genuine dispute of material fact initially rests with the moving party. Celotex Corp. v. Catrett, 106 S. Ct. 2548, 2553 (1986) (requiring the moving party to set forth “the basis for its motion, and identify[] those portions of ‘the pleadings, depositions, answers to interrogatories, and admissions on file, together with the affidavits, if any,’ which it believes demonstrate an absence of a genuine issue of material fact”); Lindsay, 578 F.3d at 414 (“The party moving for summary judgment bears the initial burden of showing that there is

no material issue in dispute.”). If the moving party meets its burden, the burden then shifts to the nonmoving party to produce “specific facts” showing a “genuine issue” for trial. Celotex Corp., 106. S. Ct. at 2253; Bass v. Robinson, 167 F.3d 1041, 1044 (6th Cir. 1999). However, “Rule 56(c) mandates the entry of summary judgment . . .

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