Wells v. Johnson & Johnson

CourtDistrict Court, W.D. Oklahoma
DecidedAugust 12, 2021
Docket5:20-cv-01301
StatusUnknown

This text of Wells v. Johnson & Johnson (Wells v. Johnson & Johnson) is published on Counsel Stack Legal Research, covering District Court, W.D. Oklahoma primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Wells v. Johnson & Johnson, (W.D. Okla. 2021).

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE WESTERN DISTRICT OF OKLAHOMA

TERESA WELLS and JOSEPH WELLS, ) ) Plaintiffs, ) ) v. ) No. CIV-20-1301-R ) JOHNSON & JOHNSON, ) a New Jersey corporation; and ) ETHICON, INC., a New Jersey ) corporation, ) ) Defendants. )

ORDER

Before the Court is Defendants Johnson & Johnson and Ethicon, Inc.’s (“Defendants”) Motion for Partial Dismissal, Doc. Nos. 37 & 38. Plaintiffs’ Teresa Wells and Joseph Wells (“Plaintiffs”) responded in opposition in Doc. No. 39. Defendants then filed a reply in support of their position. Doc. No. 42. Gynecare Gynemesh PS (“Gynemesh”) is a pelvic mesh implant “design[ed], develop[ed], promot[ed], [etc.]” to Plaintiffs by Defendants. Doc. No. 36 ¶ 8. According to the First Amended Complaint, Gynemesh contains surgical mesh that is “intended to treat [ ] pelvic organ prolapse…”. Id. ¶ 9. Gynemesh contains polypropylene mesh, which Plaintiffs state “is biologically incompatible with human tissue and […] can contribute to the formation of severe adverse reactions.” Id. ¶ 14. Defendants allegedly marketed Gynemesh “as a safe, effective, reliable medical device; implanted by safe and effective, minimally invasive surgical techniques for the treatment of medical conditions, including vaginal prolapse[.]” Id. ¶ 15. Teresa Wells received the Gynemesh implant on June 4, 2007 “to treat her pelvic organ prolapse.” Id. ¶ 9. Wells subsequently developed complications from Gynemesh, including

mesh implant complications necessitating removal due to mesh erosion, mesh degradation, mesh contracture/shrinkage[…,] worsening mixed incontinence, pelvic and abdominal pain, dyspareunia, voiding dysfunction and urinary retention, dysuria, frequency, nocturia, urinary tract infections, urgency, urinary hesitancy, vaginal scarring and fibrosis, and stress and anxiety.

Id. ¶ 10. On May 15, 2017, Wells “underwent an excision procedure to treat Gynemesh [ ] that was eroding into her rectum and not alleviating her [prolapse].” Id. ¶ 11. Plaintiffs allege that Gynemesh’s defective propensities caused the mesh erosion. Id. ¶¶ 10–14. Seeking to recover for Wells’s “severe and debilitating complications caused by Defendants’ Gynemesh[,]” Doc. No. 39, p. 1, Plaintiffs filed the following causes of actions against Defendants: (i) Negligence, (ii) Design Defect, (iii) Manufacturing Defect, (iv) Failure to Warn, (v) Fraud, (vi) Breach of Express Warranty, (vii) Breach of Implied Warranty, (viii) Constructive Fraud, (ix) Negligent Misrepresentation, (xi) Unjust Enrichment, (xii) Loss of Consortium, and (xiii) Punitive Damages. See generally Doc. No. 36. Defendants then moved to dismiss the Manufacturing Defect (iii); Breach of Express and Implied Warranty (vi and vii); Fraud (v), Constructive Fraud (viii) and Negligent Misrepresentation (ix); Unjust Enrichment (xi); and Punitive Damages (xiii) claims. See generally Doc. No. 38. In considering a Motion to Dismiss under Rule 12(b)(6), the Court must determine whether a plaintiff has stated a claim upon which relief may be granted. The motion is properly granted when the Complaint provides no “more than labels and conclusions, and a formulaic recitation of the elements of a cause of action.” Bell Atl. Corp. v. Twombly, 550 U.S. 544, 555 (2007). The Complaint must contain enough “facts to state a claim to

relief that is plausible on its face,” id. at 570, and the factual allegations “must be enough to raise a right to relief above the speculative level.” Id. at 555 (citations omitted). The Court must accept all the well-pled allegations of the Complaint as true and must construe the allegations in the light most favorable to Plaintiff. Id.; Alvarado v. KOB–TV, L.L.C., 493 F.3d 1210, 1215 (10th Cir. 2007). But the Court need not accept as true those

allegations that are conclusory in nature. Erikson v. Pawnee Cnty. Bd. of Cnty. Comm’rs, 263 F.3d 1151, 1154–55 (10th Cir. 2001). “[C]onclusory allegations without supporting factual averments are insufficient to state a claim upon which relief can be based.” Hall v. Bellmon, 935 F.2d 1106, 1109–10 (10th Cir. 1991). I. Manufacturing Defect (iii)

Defendants argue that the Amended Complaint fails to state a manufacturing defect claim because it does not allege how the Gynemesh implanted in Wells deviated from the “other Gynemesh [ ] devices that were manufactured…”. Doc. No. 38, p. 4. Plaintiffs argue that a manufacturing defect existed because the “process by which the Gynemesh [ ] was cut [ ] created unintended sharp edges” and did not contain a sheath. Doc. No. 39, pp. 3–4.

To state a manufacturing defect claim in Oklahoma, a plaintiff must allege that the defective product somehow deviated from its intended design. See Wheeler v. HO Sports Inc., 232 F.3d 754, 756 (10th Cir. 2000) (emphasis added); see also Kimbrell v. Zenith Radio Corp., 555 P.2d 590, 593 (Okla. 1976) (“[W]e hold that it did not trace the defect to the defendant-manufacturer, and therefore did not present a prima facie case.”). Here, Plaintiffs’ allegations are more akin to a design defect, and thus, fail to state

a claim for a manufacturing defect. Plaintiffs argue that similar to the complaint in Recker v. C.R. Bard, Inc., 491 F. Supp. 3d 1029, 1034 (W.D. Okla. 2020), the Amended Complaint adequately states a manufacturing defect claim. Doc. No. 39, pp. 3–4. However, in Recker, the complaint provided “that the PowerPort implanted in him differed from [the] Defendants’ intended result and/or from other ostensibly identical unit[s] of the same

product line, and varied from its intended specifications.” 491 F. Supp. 3d at 1034 (internal citations omitted). Here, however, the Plaintiffs do not allege that the specific implant that Wells received suffered from a defect. Rather, the Plaintiffs allege a defect in Gynemesh’s product specifications—i.e., that it did not contain a sheath and that cutting the products creates unintended sharp edges. Such allegations allege a defect in Gynemesh’s design, not

in the manufacturing of the specific Gynemesh causing Plaintiff’s injury. For this reason, Plaintiffs failed to state a claim upon which relief can be granted, and therefore, the manufacturing defect claim is hereby DISMISSED. II. Breach of Express and Implied Warranty (vi and vii) The Amended Complaint alleges that the Defendants breached both an express and

implied warranty. Doc. No. 36, pp. 22, 24. Defendants argue that the breach of warranty claims should be dismissed because they are time-barred and that even if they were timely, the Plaintiffs fail to identify express statements made by Defendants that Plaintiffs relied on. Doc. No. 38, pp. 5–8. In response, Plaintiffs argue that the doctrine of fraudulent concealment permits equitable tolling of its claims and that the Amended Complaint states sufficient facts to underlie its breach of warranty claims. Doc. No. 39, pp. 4–5. Fraudulent concealment may permit equitable tolling for breach of warranty claims.

See Okla. Stat. tit. 12A § 2-725(4) (“This section does not alter the law on tolling of the statute of limitations....”); see also Kinzer v. Remington Arms Co., Inc., No. CIV-09-1242- R, 2010 WL 11451121 at *5 (W.D. Okla. Sept. 1, 2010); AG Equip. Co. v. AIG Life Ins. Co., No 07–CV–0556–CVE–PJC, 2008 WL 4570319, at *3 (N.D. Okla. Oct. 10, 2008) (“[F]raudulent concealment is typically raised as a response to a statute of limitations

defense […]”).

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Wells v. Johnson & Johnson, Counsel Stack Legal Research, https://law.counselstack.com/opinion/wells-v-johnson-johnson-okwd-2021.