Kuchenbecker v. Johnson & Johnson

CourtDistrict Court, S.D. Florida
DecidedSeptember 16, 2019
Docket0:19-cv-61712
StatusUnknown

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

Bluebook
Kuchenbecker v. Johnson & Johnson, (S.D. Fla. 2019).

Opinion

UNITED STATES DISTRICT COURT FOR THE SOUTHERN DISTRICT OF FLORIDA Miami Division Case Number: 19-61712-CIV-MORENO CORRINE KUCHENBECKER and THOMAS KUCHENBECKER, Plaintiffs, Vs. JOHNSON & JOHNSON, and ETHICON, INC. Defendants. / ORDER GRANTING IN PART AND DENYING IN PART DEFENDANTS’ PARTIAL MOTION TO DISMISS Plaintiffs Corrine Kuchenbecker and Thomas Kuchenbecker commenced this lawsuit against Defendants Johnson & Johnson and Ethicon, Inc., seeking compensatory, economic, and punitive damages for injuries caused by complications from a transvaginal mesh device, known as the Gynecare TVT Abbrevo System, which was implanted in Plaintiff Corrine Kuchenbecker. The Plaintiffs’ core claim is that the Defendants are liable in negligence and strict liability for defectively designing and manufacturing the Gynecare TVT Abbrevo System, and for failing to adequately warn consumers of known dangers and risks associated with using this system. Defendants moved to dismiss certain claims in the 12-count Complaint as failing to state a claim upon which relief can be granted under Federal Rule of Civil Procedure 12(b)(6). For the reasons below, Defendants’ Partial Motion to Dismiss is GRANTED IN PART AND DENIED IN PART.

I, LEGAL STANDARD A motion to dismiss under Federal Rule of Civil Procedure 12(b)(6) tests the formal sufficiency of the allegations supporting claims for relief. Under Rule 12(b)(6), the Court “may dismiss a claim for ‘failure to state a claim upon which relief can be granted.’” Tello v. Royal Caribbean Cruises, Ltd., 939 F. Supp. 2d 1269, 1275 (S.D. Fla. 2013) (quoting Fed. R. Civ. P. 12(b)(6)). To survive dismissal, the Complaint “must contain sufficient factual matter, accepted as true, to ‘state a claim to relief that is plausible on its face.’”” Ashcroft v. Iqbal, 556 U.S. 662, 678 (2009) (quoting Bell Atlantic Corp. v. Twombly, 550 U.S. 544, 570 (2007)). “A claim has facial plausibility when the plaintiff pleads factual content that allows the court to draw the reasonable inference that the defendant is liable for the misconduct alleged.” Jd. “While legal conclusions can provide the framework of a complaint, they must be supported by factual allegations.” Iqbal, 556 U.S. at 679. And those “[flactual allegations must be enough to raise a right to relief above the speculative level.” Twombly, 550 U.S. at 555. When ruling on a motion to dismiss, a court must view the complaint in the light most favorable to the plaintiff and accept the plaintiff's well-pleaded facts as true. See St. Joseph’s Hosp., Inc. v. Hosp. Corp. of Am., 795 F.2d 948, 954 (11th Cir. 1986). Il, DISCUSSION A. COUNTS I AND III - “DEFECTIVE MANUFACTURING” The thrust of Plaintiffs’ lawsuit is that the Defendants are liable in negligence and strict liability for defectively designing and manufacturing the Gynecare TVT Abbrevo System, and for failing to adequately warn consumers of known dangers and risks associated with using this system. Defendants request dismissal of the defective manufacturing claims in Counts I and II on grounds the Complaint amounts to “nothing more than a formulaic recitation of elements, bereft of factual support.” (D.E. 5 at 4.) -2-

Plaintiffs’ defective manufacturing claims fall into two theories of liability: negligence and strict liability. The basic elements of a negligence cause of action apply equally to products liability manufacturing defect claims grounded in negligence. See Colville v. Pharmacia & Upjohn Co. LLC, 565 F. Supp. 2d 1314, 1320 (N.D. Fla. 2008). A plaintiff must allege: (1) a duty of care was owed to the plaintiff; (2) defendant breached that duty of care (i.e. negligence); and (3) the breach of that duty of care was a proximate cause of the plaintiff's injuries. /d. In addition to these elements, a plaintiff must also establish that the product at issue was “defective or unreasonably dangerous.” /d. (quoting Marzullo v. Crosman Corp., 289 F. Supp. 2d 1337, 1342 (M.D. Fla. 2003)). Likewise, a manufacturing defect claim grounded in strict liability requires that a plaintiff prove the product made by the manufacturer was defective or created an unreasonably dangerous condition that proximately caused the plaintiffs injury. Id. (quoting McCorvey v. Baxter Healthcare Corp., 298 F.3d 1253, 1258 (11th Cir. 2002)). And finally, under both theories of liability, a plaintiff must also demonstrate that “the injuries complained of were caused by a defective product whose defect existed at the time of injury and at the time in which the product left the manufacturer’s control.” Jd. (quoting Rodriguez v. Nat'l Detroit, Inc., 857 So. 2d 199, 201 (Fla. 3d DCA 2003)). Here, the Court finds the Complaint fails to state a plausible claim for defective manufacturing under negligence and strict liability. The closest Plaintiffs come to alleging a manufacturing defect is the allegation that Defendants failed to “manufacture the Gynecare TVT Abbrevo System so as to avoid an unreasonable risk of harm to women in whom the Gynecare TVT Abbrevo System[s] were implanted, including the Plaintiff.” (D.E. 1 at §116b.) But the only factual allegations offered to support this conclusion relate to the defective design and defective warning claims. See id. at J] 62a—62i, 74a-74r. And without pinpointing a single specific manufacturing defect (i.e. that the Gynecare TVT Abbrevo System, as manufactured, -3-

deviated from the manufacturing specifications in some way), and explaining how that defect caused any of the alleged injuries, this allegation is simply another way of alleging defective design. The Complaint does allege that the Gynecare TVT Abbrevo System was “defective in its manufacture and construction when it left the hands of [Defendants] in that it deviated from Gynecare TVT Abbrevo System specifications.” Jd. at ¢ 125. But, again, the Complaint fails to specify how the device implanted in the Plaintiff deviated from manufacturing specifications. Without more, the Court simply cannot draw the reasonable inference that Defendants defectively manufactured the Gynecare TVT Abbrevo System that was implanted in the Plaintiff. Therefore, even taking these allegations as true and viewing them in the light most favorable to Plaintiffs, the Court finds that Plaintiffs fail to allege a plausible manufacturing defect claim grounded in negligence or strict liability. Accordingly, Count I is DISMISSED to the extent it asserts a manufacturing defect claim,! and Count III is DISMISSED in its entirety. B. COUNT IV - “STRICT LIABILITY - DEFECTIVE PRODUCT” In Count IV, Plaintiffs assert a strict liability claim for “defective product” on grounds the Gynecare TVT Abbrevo System was “defective and unreasonably dangerous to foreseeable consumers, patients, and users.” Jd. at [{ 128-32. Defendants argue Count IV should be dismissed because Florida does not recognize “defective product” as a separate cause of action.

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Bluebook (online)
Kuchenbecker v. Johnson & Johnson, Counsel Stack Legal Research, https://law.counselstack.com/opinion/kuchenbecker-v-johnson-johnson-flsd-2019.