Durham v. Johnson & Johnson

CourtDistrict Court, E.D. Tennessee
DecidedAugust 24, 2021
Docket3:20-cv-00554
StatusUnknown

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

Bluebook
Durham v. Johnson & Johnson, (E.D. Tenn. 2021).

Opinion

UNITED STATES DISTRICT COURT EASTERN DISTRICT OF TENNESSEE AT KNOXVILLE

BRENDA DURHAM, ) ) Plaintiff, ) Case No. 3:20-CV-554 ) v. ) Judge Collier ) JOHNSON & JOHNSON and ) Magistrate Judge Poplin ETHICON, INC., ) ) Defendants. )

M E M O R A N D U M

Before the Court is a motion by Defendants, Johnson & Johnson and Ethicon, Inc., to dismiss the First Amended Complaint (Doc. 11) of Plaintiff, Brenda Durham, pursuant to Rule 12(b)(6) of the Federal Rules of Civil Procedure. (Doc. 18.) Plaintiff has filed a response in opposition (Doc. 21), as well as a supplemental brief (Doc. 23), and Defendants have replied (Doc. 22), as well as filed a response to Plaintiff’s supplemental brief (Doc. 24). For the following reasons, the Court will GRANT Defendants’ motion to dismiss (Doc. 18). I. BACKGROUND The following summary of the facts accepts all factual allegations in Plaintiff’s First Amended Complaint (Doc. 11) as true. See Gunasekera v. Irwin, 551 F.3d 461, 466 (6th Cir. 2009). A. Defendants’ Pelvic-Mesh Product Defendants designed, manufacture, and market the TVT-Obturator (the “TVT-O”), a pelvic-mesh product that is implanted in women who suffer from stress urinary incontinence to repair weakened or damaged tissue in the vagina. The TVT-O is made from polypropylene mesh and/or collagen. Polypropylene mesh is biologically incompatible with human tissue. As a result, it degrades in tissue upon implantation, which can cause severe adverse reactions like inflammation of the pelvic tissue, nerve entrapment due to the contraction of the mesh, and chronic pain, among other issues. If the TVT-O is comprised of collagen, the collagen can disintegrate into a woman’s pelvis, leading to the hardening of tissue, chronic pain, and fibrotic reaction. The use of polypropylene mesh and collagen make the TVT-O defective. But the product

also is defective due to where it is inserted in the tissue; biomechanical issues that cause the mesh to contract; its propensity for plastic deformation, rigidity, and inflexibility; degradation and fragmentation; and the difficulty of its removal. Defendants are aware of these defects and the risks associated with them. Even so, Defendants market the TVT-O to healthcare providers and patients as a device that can be implanted through a minimally invasive procedure and that results in minimal local tissue reactions and trauma. The Food and Drug Administration (the “FDA”) had previously cleared the TVT-O for sale in the United States, although such clearance did not require Defendants to prove the safety and efficacy of the product. However, on October 20, 2008, the FDA issued a notification

regarding over a thousand complaints regarding pelvic-mesh products, including the TVT-O. On July 13, 2011, the FDA issued a warning for serious complications associated with pelvic-mesh products used for pelvic organ prolapse (“POP”) repair, which use the same mesh as the TVT-O. On April 16, 2019, the FDA ordered all transvaginal POP device manufacturers to stop selling and distributing their POP products. As of February 17, 2021, the FDA has not banned the sale and distribution of Defendants’ TVT-O, although the TVT-O uses the same mesh as the POP devices. To this day, Defendants market the TVT-O to the medical community and patients as a safe, effective, and reliable medical device. B. Plaintiff’s TVT-O Implant On October 12, 2011, Plaintiff was implanted with a TVT-O by Dr. Lee Congleton, III, in Knoxville, Tennessee. At some point after the implant, Plaintiff developed complications from her TVT-O and experienced pelvic pain, pelvic relaxation, mixed incontinence, hesitancy, frequency, and dyspareunia. Plaintiff has sought medical treatment for these complications and

likely will need to do so in the future as well. C. Procedural History On December 30, 2020, Plaintiff filed this lawsuit against Defendants. (Doc. 1.) On February 17, 2021, Plaintiff filed her First Amended Complaint, asserting ten claims against Defendants: (1) general negligence, failure to warn or instruct, negligent infliction of emotional distress, and gross negligence under the Tennessee Products Liability Act (the “TPLA”), Tenn. Code Ann. §§ 29-28-101, et seq.; (2) negligent misrepresentation; (3) strict liability due to design defect, manufacturing defect, failure to warn, and defective product under the TPLA; (4) breach of express warranty; (5) breach of implied warranty under the TPLA; (6) fraud; (7) constructive

fraud; (8) fraudulent concealment under the TPLA; (9) unjust enrichment under the TPLA; and (10) punitive damages. (Doc. 11 ¶¶ 76–191.) Defendants move to dismiss the First Amended Complaint under Rule 12(b)(6) of the Federal Rules of Civil Procedure. (Doc. 18.) As an initial matter, Defendants contend Plaintiff’s claims must be dismissed due to her failure to conform those claims with the TPLA, specifically that she pleaded them as separate counts. (Doc. 19 at 3–5.) Alternatively, Defendants argue Plaintiff has failed to state any claim for relief, as she fails to plausibly allege the elements of a TPLA claim for three reasons. (Id. at 6–20.) First, Defendants assert Plaintiff’s allegations of design defect are vague and conclusory and fail to allege causation. (Id. at 6–9.) Second, Defendants argue Plaintiff has not alleged a manufacturing defect because she has not alleged either causation or how the manufacturing of her TVT-O deviated from other TVT-Os. (Id. at 9– 10.) Third, Defendants contend Plaintiff’s failure-to-warn theory fails because she does not plead how the warnings were inadequate or how the inadequate warnings injured her. (Id. at 10–12.) Alternatively, Defendants argue some of Plaintiff’s claims fail on additional grounds other than

the TPLA. (Id. at 12–20.) Finally, Defendants assert Plaintiff’s claim for punitive damages should be dismissed because it is not an independent cause of action under Tennessee law. (Id. at 20.) Plaintiff has responded in opposition, arguing she has pleaded claims consistent with the TPLA and has discretion to assert separate TPLA claims. (Doc. 21 at 3–4.) Plaintiff also contends she has alleged plausible claims based on design defect, manufacturing defect, and failure to warn. (Id. at 4–6.) Plaintiff argues several of her claims are not subsumed by the TPLA and she has adequately pleaded those claims. (Id. at 6–12.) In addition, Plaintiff asserts Tennessee recognizes a claim for punitive damages as a separate claim. (Id. at 12–13.) Finally, Plaintiff asks the Court for leave to file an amended complaint if it finds Defendants’ motion meritorious. (Id. at 13.)

Defendants have filed a reply, in which they reiterate their principal arguments for dismissal. (Doc. 22.) Plaintiff has filed a supplemental brief addressing a recent decision from the United States District Court for the Western District of Oklahoma (Doc. 23), to which Defendants filed a reply (Doc. 24). Defendants’ motion to dismiss is now ripe for review. II. STANDARD OF REVIEW A party may move to dismiss a claim for failure to state a claim upon which relief can be granted. Fed. R. Civ. P. 12(b)(6). In deciding a Rule 12(b)(6) motion to dismiss, a court first must accept all factual allegations of the complaint as true and construe the complaint in the light most favorable to the plaintiff. See Grindstaff v. Green, 133 F.3d 416, 421 (6th Cir. 1998).

Free access — add to your briefcase to read the full text and ask questions with AI

Related

Papasan v. Allain
478 U.S. 265 (Supreme Court, 1986)
Bell Atlantic Corp. v. Twombly
550 U.S. 544 (Supreme Court, 2007)
Ashcroft v. Iqbal
556 U.S. 662 (Supreme Court, 2009)
Susie J. Jackson v. Richards Medical Company
961 F.2d 575 (Sixth Circuit, 1992)
Sigler v. American Honda Motor Co.
532 F.3d 469 (Sixth Circuit, 2008)
Gunasekera v. Irwin
551 F.3d 461 (Sixth Circuit, 2009)
Liberty Mutual Insurance Company v. Stevenson
368 S.W.2d 760 (Tennessee Supreme Court, 1963)
King v. Danek Medical, Inc.
37 S.W.3d 429 (Court of Appeals of Tennessee, 2000)
Oakley v. Simmons
799 S.W.2d 669 (Court of Appeals of Tennessee, 1990)
Maness v. Boston Scientific
751 F. Supp. 2d 962 (E.D. Tennessee, 2010)
Charolette Payne v. Novartis Pharm. Corp.
767 F.3d 526 (Sixth Circuit, 2014)
Lea Ann Tatham v. Bridgestone Americas Holding, Inc.
473 S.W.3d 734 (Tennessee Supreme Court, 2015)
Victoria Jackson v. Ford Motor Company
842 F.3d 902 (Sixth Circuit, 2016)
Grindstaff v. Green
133 F.3d 416 (Sixth Circuit, 1998)
Fleming v. Janssen Pharmaceuticals, Inc.
186 F. Supp. 3d 826 (W.D. Tennessee, 2016)
Moore v. C.R. Bard, Inc.
217 F. Supp. 3d 990 (E.D. Tennessee, 2016)

Cite This Page — Counsel Stack

Bluebook (online)
Durham v. Johnson & Johnson, Counsel Stack Legal Research, https://law.counselstack.com/opinion/durham-v-johnson-johnson-tned-2021.