Simmons v. Cardinal Health, Inc.

CourtDistrict Court, E.D. Louisiana
DecidedNovember 20, 2020
Docket2:20-cv-02174
StatusUnknown

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

Bluebook
Simmons v. Cardinal Health, Inc., (E.D. La. 2020).

Opinion

UNITED STATES DISTRICT COURT EASTERN DISTRICT OF LOUISIANA

JESSIE SIMMONS CIVIL ACTION

VERSUS NO: 20-2174

CARDINAL HEALTH, INC., et al SECTION: “J”(2)

ORDER AND REASONS

Before the Court is a Motion to Dismiss (Rec. Doc. 9) filed by Defendants, Cardinal Health 200, LLC and Cardinal Health, Inc (collectively “Cardinal Health”). Plaintiff, Jessie Simmons, opposes the motion. (Rec. Doc. 15). Defendants filed a reply (Rec. Doc. 22). Having considered the motion and legal memoranda, the record, and the applicable law, the Court finds that the motion should be GRANTED in part and DENIED in part. FACTS AND PROCEDURAL HISTORY

Defendants in this case designed, manufactured, tested, marketed, promoted, and sold a high viscosity bone cement known as Cardinal Health Arthroplasty Bone Cement (hereinafter “Cardinal HV”), which was intended to be used in total knee arthroplasties. The bone cement is used to attach artificial knee joints to the femur and tibia. Bone cement may be low, medium, or high viscosity, but all three types of bone cements have the same intended use and are used interchangeably. On February 28, 2018, Plaintiff received a total knee arthroplasty in which Cardinal HV was used. Plaintiff alleges that he was forced to undergo a revision surgery on August 7, 2019 due to the defectiveness of Defendants’ Cardinal HV. Specifically, Plaintiff alleges that Defendants’ Cardinal HV failed due to mechanical loosening. Plaintiff also alleges that high viscosity bone cements, such as Cardinal

HV, have been proven worse than lower viscosity bone cements because they fail more often and have an increased risk of mechanical loosing. On August 4, 2020, Plaintiff filed the present action against Defendants, primarily alleging that Defendants violated the Louisiana Products Liability Act (“LPLA”) due to a design defect, construction or composition defect, and breach of express warranty. Plaintiff also alleges that Defendants breached the warranty

against redhibitory defects. In response, Defendants filed the instant motion to dismiss. LEGAL STANDARD

Under the Federal Rules of Civil Procedure, a complaint must contain “a short and plain statement of the claim showing that the pleader is entitled to relief.” Fed. R. Civ. P. 8(a)(2). The complaint must “give the defendant fair notice of what the claim is and the grounds upon which it rests.” Dura Pharm., Inc. v. Broudo, 544 U.S. 336, 346 (2005) (internal citations omitted). The allegations “must be simple, concise, and direct.” Fed. R. Civ. P. 8(d)(1). “Under Rule 12(b)(6), a claim may be dismissed when a plaintiff fails to allege any set of facts in support of his claim which would entitle him to relief.” Taylor v. Books A Million, Inc., 296 F.3d 376, 378 (5th Cir. 2002) (citing McConathy v. Dr. Pepper/Seven Up Corp., 131 F.3d 558, 561 (5th Cir. 1998)). To survive a Rule 12(b)(6) motion to dismiss, the plaintiff must plead enough facts to “state a claim to relief that is plausible on its face.” Ashcroft v. Iqbal, 556 U.S. 662, 678 (2009) (quoting Bell Atl. Corp. v. Twombly, 550 U.S. 544, 570 (2007)). A claim is facially plausible when the

plaintiff pleads facts that allow the court to “draw the reasonable inference that the defendant is liable for the misconduct alleged.” Id. A court must accept all well- pleaded facts as true and must draw all reasonable inferences in favor of the plaintiff. Lormand v. U.S. Unwired, Inc., 565 F.3d 228, 232 (5th Cir. 2009); Baker v. Putnal, 75 F.3d 190, 196 (5th Cir. 1996). The court is not, however, bound to accept as true legal conclusions couched as factual allegations. Iqbal, 556 U.S. at 678. “[C]onclusory

allegations or legal conclusions masquerading as factual conclusions will not suffice to prevent a motion to dismiss.” Taylor, 296 F.3d at 378. DISCUSSION

I. DESIGN DEFECT First, Defendants argue that Plaintiff failed to state a design defect claim because Plaintiff did not allege the existence of an alternative design. After establishing that a product caused damage through a reasonably anticipated use, a plaintiff alleging a design defect must prove: “(1) there existed an alternative design that was capable of preventing the claimant's damage, and (2) the risk avoided by the alternative design outweighed the burden of its adoption by the manufacturer and any adverse effect the alternative design would have on the product's utility.” Marable v. Empire Truck Sales of Louisiana, LLC, 2016-0876 (La. App. 4 Cir. 6/23/17), 221 So. 3d 880, 895 (citing LA. REV. STAT. § 9:2800.56). In this case, Plaintiff alleges that a low or medium viscosity bone cement is a safer reasonable alternative design to high viscosity bone cement. (Rec. Doc. 1, at ¶26-29). Specifically, Plaintiff alleges that lower viscosity bone cement designs are

safer than Cardinal HV because Cardinal HV suffers from “significantly increased variations in application and setting times.” (Rec. Doc. 1, at ¶37). In support of Plaintiff’s allegations, Plaintiff argues that the Orthopaedic Research Society and Journal of Arthroplasty have published research showing that high viscosity bone cement is less effective than lower viscosity bone cement, due to increased risk of failure. (Rec. Doc. 1, at ¶¶ 26-27). In their motion to dismiss, Defendants argue that

low or medium viscosity bone cements are not an alternative design to high viscosity bone cements, but instead, they are an entirely different product. (Rec. Doc. 9, at p. 5). Thus, this argument turns on where the line is drawn between an alternative design of a product and an entirely different product. In support of their argument, Defendants cite Theriot v. Danek Medical, Inc., where the Fifth Circuit Court of Appeals examined this issue with regards to the use of pedicle screws for biomechanical stability. 168 F.3d 253, 255 (5th Cir. 1999). In

that case, the plaintiff raised two separate arguments. Id. at 255-56. First, the plaintiff argued that all pedicle screws were an alternative design to other classes of product that provide biomechanical stability, “such as external neck braces or internal systems that use hooks or wires.” Id. at 255. The Fifth Circuit rejected this argument, holding that this was an issue with the physician’s choice of treatment, rather than the design of the product. Id. In the alternative, the plaintiff also argued that there were alternative pedicle screw designs that would have prevented his injury. Id. Although the Fifth Circuit rejected this argument because it had not been raised to the district court, the Fifth Circuit noted that an alternative pedicle screw

design may have existed that supported the plaintiff’s claim. Id.

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Related

Baker v. Putnal
75 F.3d 190 (Fifth Circuit, 1996)
Taylor v. Books a Million, Inc.
296 F.3d 376 (Fifth Circuit, 2002)
Lormand v. US Unwired, Inc.
565 F.3d 228 (Fifth Circuit, 2009)
Dura Pharmaceuticals, Inc. v. Broudo
544 U.S. 336 (Supreme Court, 2005)
Bell Atlantic Corp. v. Twombly
550 U.S. 544 (Supreme Court, 2007)
Ashcroft v. Iqbal
556 U.S. 662 (Supreme Court, 2009)
Lyles v. Medtronic Sofamor Danek, USA, Inc.
871 F.3d 305 (Fifth Circuit, 2017)
Marable v. Empire Truck Sales of Louisiana, LLC
221 So. 3d 880 (Louisiana Court of Appeal, 2017)

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