Killen v. Johnson & Johnson

CourtDistrict Court, S.D. Mississippi
DecidedFebruary 3, 2022
Docket3:20-cv-00829
StatusUnknown

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

Bluebook
Killen v. Johnson & Johnson, (S.D. Miss. 2022).

Opinion

UNITED STATES DISTRICT COURT SOUTHERN DISTRICT OF MISSISSIPPI NORTHERN DIVISION

MARY KILLEN and MICHAEL KILLEN PLAINTIFFS

V. CIVIL ACTION NO. 3:20-CV-829-KHJ-MTP

JOHNSON & JOHNSON and ETHICON, INC. DEFENDANTS

ORDER This action is before the Court on Defendants Johnson & Johnson and Ethicon, Inc.’s (“Defendants”) Motion for Partial Dismissal of Plaintiffs’ Second Amended Complaint [16]. As explained below, the Court grants in part and denies in part Defendants’ motion. I. Facts and Procedural History Plaintiffs Mary and Michael Killen allege that Mrs. Killen sustained injuries from the implantation of the TVT-Obturator (“TVT-O”) pelvic mesh device manufactured by Defendant Ethicon, Inc. for the surgical treatment of stress urinary incontinence. Second Am. Compl. [15]. The Killens contend that, following implantation of the TVT-O mesh, the mesh eroded and caused Mrs. Killen chronic injuries by degrading, shrinking, contracting, migrating, and deforming. . ¶ 7. They also allege the TVT-O device’s mesh is incompatible with human tissue and promotes immune responses in large swaths of the population. ¶ 22. Following an immune response, the TVT-O’s degradation causes chronic inflammation, nerve entrapment, infectious disease response, and chronic pain. ¶ 23–24. The Killens contend that, at all times relevant to Mrs. Killen receiving the device, Defendants knew of the TVT-O’s defective condition. They assert Defendants marketed the product with knowledge of the defects and mislead the medical community as to the

risks associated with the material. ¶¶ 28–30. The Killens sue for (I) design defect, (II) manufacturing defect, (III) failure to warn, (IV) breach of express warranty, (V) failure to conform to representations, and (VI) unjust enrichment, seeking compensatory and punitive damages, and equitable relief. [15] ¶¶ 90–185. Mr. Killen also brings a loss of consortium claim. . ¶¶ 186–92. Defendants move to dismiss the Killens’ claims for manufacturing

defect (Count II), breach of express warranty (Count IV), failure to conform to representations (Count V), and unjust enrichment (Count VI) claims under Rule 12(b)(6) for failure to state a claim. [16]. II. Standard In reviewing a Rule 12(b)(6) motion, the Court, viewing all evidence in the light most favorable to the plaintiff, must consider whether the plaintiff states a valid claim for relief. , 528 F.3d 413, 418 (5th Cir. 2008). To

state a valid claim for relief, the plaintiff must allege enough facts that, when accepted as true, show “facial plausibility” and allow “the court to draw the reasonable inference that the defendant is liable for the misconduct alleged.” , 556 U.S. 662, 678 (2009) (citing , 550 U.S. 544, 556 (2007)). The plaintiff need not provide detailed factual allegations to survive a Rule 12(b)(6) motion but must allege enough facts “to raise a right of relief above the speculative level.” , 550 U.S. at 555. The Court need not accept as true a plaintiff’s legal conclusions or “threadbare recitals of the elements of a cause of action, supported by mere conclusory statements.” , 556 U.S. at 678

(citing , 550 U.S. at 555). III. Analysis Defendants ask the Court to dismiss these claims from Killens’ Second Amended Complaint: Count II, manufacturing defect; Count IV, breach of express warranty; Count V, failure to conform to representations; and Count VI unjust enrichment. The Court addresses each claim separately.

A. Count II: Manufacturing Defect Defendants argue that the manufacturing defect claim fails because the Killens do not allege that the type of mesh used in Killen’s TVT-O implant differed from the mesh used in other TVT-O devices. [17] at 3. Defendants also argue that the Killens do not plead enough facts showing that the TVT-O implant deviated from Ethicon’s design specifications. The Killens contend that the TVT-O product implanted in Mrs. Killen was manufactured in a defective manner because

the manufacturer failed to: (1) use biologically compatible mesh material; (2) provide adequate specifications in design; (3) cut the mesh without sharp edges, and; (4) to include a protective sheath. [15] ¶¶ 104–09. To succeed on a claim for manufacturing defect under the Mississippi Products Liability Act, a party must prove these elements existed “at the time the product left the control of the manufacturer”: (i) [t]he product was defective because it deviated in a material way from the manufacturer’s or designer’s specifications or from otherwise identical units manufactured to the same manufacturing specifications, . . . (ii) the defective condition rendered the product unreasonably dangerous to the user or consumer; and (iii) the defective and unreasonably dangerous condition of the product proximately caused the damages for which recovery is sought.

Miss. Code Ann. § 11-1-63(a)(1). Manufacturing defect claims involve allegations that the specific product the consumer bought was manufactured in a way that deviated from the design specification. , 991 F. Supp. 2d 778, 780 (N.D. Miss. 2014). A party must plead how the subject product deviated from the manufacturer’s specifications or other units, or the claim must be dismissed. Inc., No. 3-12-CV-797, 2013 WL 1791373, at *3 (S.D. Miss. Apr. 19, 2013). The Killens fail to sufficiently plead a manufacturing defect. The Killens may state a claim for a manufacturing defect by claiming Mrs. Killen’s TVT-O was materially different from other TVT-O’s or by claiming the device deviated from design specifications. Miss. Code Ann. § 11-1-63(a)(1)(i). They assert the second theory. [15], ¶ 100. To support this theory, the Killens allege the TVT-O implant did not conform to Ethicon’s intended design by (1) using non-medical grade material, . ¶ 104, (2) being cut by a laser or machine that caused the polypropylene mesh to have sharp edges, . ¶ 107, and (3) not having a sheath, which created an abrasive insertion and lead to mesh erosion, . ¶ 108. None of these allegations support a theory of manufacturing defect because the Killens admit Defendants designed the TVT-O to use polypropylene mesh, ¶ 20, and do not allege that Defendants designed the TVT-O to have a sheath. And the Killens do not allege design specifications requiring particular methods in cutting the TVT-O mesh or prohibiting the use of a laser or machine in the process. For these reasons,

the Court dismisses the Killens’ manufacturing defect claim. B. Count IV: Breach of Express Warranty The Killens argue Defendants made and breached express warranties to them and their physician about the quality and safety of the device in advertisements, marketing materials, and instructions. [15] at 133–45. Defendants assert that this claim is time-barred and, even if it is timely, the Killens identify no

express warranty or representations Defendants made to them. [17] at 5–11. The Killens counter that the discovery rule and Defendants’ acts of fraudulent concealment tolled the statute of limitations, rendering their claim timely. Alternatively, the Killens assert that Defendants waived or should be equitably estopped from asserting their limitations argument. [15] at 79–89. a. Statute of Limitations When a defendant asserts a statute of limitations defense,1 the Court may

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Bluebook (online)
Killen v. Johnson & Johnson, Counsel Stack Legal Research, https://law.counselstack.com/opinion/killen-v-johnson-johnson-mssd-2022.