Casey v. Wright Medical Technology Incorporated

District Court, D. Arizona·Decided February 13, 2020·No. 2:19-cv-05360·Unknown

Opinion

WO

IN THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF ARIZONA

Theresa I. Casey, No. CV-19-05360-PHX-NVW

Plaintiff, v. ORDER Wright Medical Technology, Inc., a foreign corporation,

Defendant.

Before the Court is Defendant Wright Medical Technology, Inc.’s (“Wright”) Partial Motion to Dismiss (Doc. 11). For the reasons stated below, the motion shall be granted in part and denied in part. I. BACKGROUND The following allegations from Plaintiff Theresa I. Casey’s (“Casey”) First Amended Complaint (Docs. 7, 7-1, and 7-2) are presumed true at this stage. See Brown v. Elec. Arts, Inc., 724 F.3d 1235, 1247 (9th Cir. 2013) (“[O]n a motion to dismiss, the court presumes that the facts alleged by the plaintiff are true.”).1 On August 18, 2008, Casey underwent a total hip arthroplasty (more commonly known as hip replacement surgery), during which Dr. Dwight S. Keller, M.D. (“Doctor

1 Unless otherwise indicated, in citing cases, all internal quotation marks, citations, emphases, alterations, and footnotes are omitted. Keller”) implanted in Casey’s right hip a variety of artificial hip devices designed, manufactured, distributed, sold, and marketed by Wright, including the product at issue here, the “Wright Profemur® Plasma Z Stem” and its neck. (Docs. 7, 7.1, and 7.2 at ¶¶ 5, 7-8, 69.) A little over a year later, after Casey began experiencing pain in her right hip, Dr. Keller conducted a total hip arthroplasty revision, during which he found the Wright artificial hip had dislocated and again implanted a variety of Wright artificial hip devices. (Id. at ¶¶ 71-73.) This procedure did not put an end to Casey’s troubles, as she had to undergo a second total hip arthroplasty revision in December 2011 due to another breakdown of the Wright artificial hip. (Id. at ¶¶ 75-76.) She underwent a third such surgery in November 2017 after the Wright artificial hip again failed. (Id. at ¶¶ 88-89.) Wright’s titanium Profemur® system is a modular hip stem and neck system. (Id. at ¶ 35.) The modular stem has a separate neck component that attaches to the top of the stem and a femoral ball which in turn attaches to the modular neck. (Id. at ¶¶ 37, 39-40.) According to Wright, “[n]o existing hip implant is better suited to address . . . the historical challenges of total hip arthroplasty.” (Id. at ¶ 41.) In marketing the Profemur® system in 2008, 2009, and 2011 to Casey, Dr. Keller, and the consuming public, Wright stated: “[t]he clinical effectiveness and dependability of the modular necks has been consistently demonstrated throughout the PROFEMUR® Hip clinical history. Utilized in both primary and revision applications, the current neck design has been successfully employed to improve surgical outcomes with no reported failures.” (Id. at ¶¶ 42, 125.) Touting the strength of the coupling between the neck and the stem, Wright further indicated:

Modular neck clinical experience and extensive laboratory tests have proven the coupling between the modular neck and femoral implant provides:

• Structural reliability • Absence of significant micromovement • Absence of fretting corrosion These excellent characteristics are obtained due to the patented geometry of the coupling. The necks are made from titanium alloy (Ti6Al4V) which is proven to afford suitable mechanical properties, ideal biocompatibility, and excellent resistance to corrosion.

(Id. at ¶¶ 43, 125.) However, Wright “did not test the Profemur® Plasma Z system for safety before its release to the public.” (Id. at ¶ 48.) Indeed, Wright marketed the system “as having a clinical history of being safe on account of the clinical history of predicate devices, not the actual device being marketed” and knew “there was no clinical evidence to support its contention that its device was safe or effective.” (Id. at ¶¶ 51-52.) On the contrary, “[t]he testing done to the product prior to the launch was woefully inadequate, unreasonable, and not representative of real-world, clinical situations.” (Id. at ¶ 50.) As it turned out, the Profemur® Plasma Z system was not the Wright stuff. The system’s titanium alloy modular neck was prone to fretting and corrosion, which in turn made it susceptible to fracture. (Id. at ¶¶ 53-55.) By 2008, Wright received a large number of reports and warnings from surgeons and others regarding the Profemur® Plasma Z system components and until 2009, the system experienced a high rate of failures worldwide. (Id. at ¶¶ 64-65.) In 2009, Wright, aware of the “high rates of problems” with the Profemur® Plasma Z system, changed the design of the modular necks “from a titanium alloy to a cobalt- chrome alloy in order to try to increase its safety and efficacy.” (Id. at ¶¶ 57, 61.) Yet, Wright did not recall the previously-issued titanium alloy modular necks and did not issue “any warning to doctors or patients who had previously received an implanted titanium modular neck.” (Id. at ¶ 59.) Moreover, in 2008, 2009, and 2011, Wright did not disclose information regarding the performance history, dangers, and risks of the Profemur® Plasma Z system to either Casey, Dr. Keller, or the consuming public. (Id. at ¶ 122.) Casey initiated this action in the Superior Court of the State of Arizona in and for Maricopa County on September 18, 2019 against Wright, as well as against Wright Medical Group, Inc. and numerous fictitious individuals and entities. (Doc. 1-3.) Defendants timely removed the action to this Court. (Doc. 1.) On October 16, 2019, Casey filed a First Amended Complaint (the “Complaint”) against Wright, which alleges four causes of action: (1) Strict Product Liability—Design Defect, (2) Strict Product Liability—Failure to Issue Post-Sale Warnings, (3) Negligence, and (4) Negligent Misrepresentation. (Docs. 7, 7-1, and 7-2.) Wright’s motion seeks an order dismissing Casey’s negligent misrepresentation cause of action and prayer for punitive damages.2 A. Pleading Standard When considering a motion to dismiss, a court evaluates the legal sufficiency of the plaintiff’s pleading. Dismissal under Federal Rule of Civil Procedure (“Rule”) 12(b)(6) can be based on the “lack of a cognizable legal theory” or “the absence of sufficient facts alleged under a cognizable legal theory.” Balistreri v. Pacifica Police Dep’t, 901 F.2d 696, 699 (9th Cir. 1990). In deciding a motion to dismiss under Rule 12(b)(6), all allegations of material fact are assumed to be true and construed in the light most favorable to the nonmoving party. Cousins v. Lockyer, 568 F.3d 1063, 1067 (9th Cir. 2009). However, this principle does not apply to legal conclusions or conclusory factual allegations. Ashcroft v. Iqbal, 556 U.S. 662, 678 (2009). “Threadbare recitals of the elements of a cause of action, supported by mere conclusory statements, do not suffice.” Id. Neither do “naked assertion[s]” devoid of “further factual enhancement.” Bell Atl. Corp. v. Twombly, 550 U.S. 544, 557 (2007). Under Rule 8(a)(2), a pleading that states a claim for relief must contain “a short and plain statement of the claim showing that the pleader is entitled to relief.” A complaint need contain only “enough facts to state a claim for relief that is plausible on its face.” Twombly, 550 U.S. at 570. “A claim has facial plausibility when the plaintiff pleads factual

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

Casey v. Wright Medical Technology Incorporated, (D. Ariz. 2020).

Casey v. Wright Medical Technology Incorporated (Casey v. Wright Medical Technology Incorporated) — published by Counsel Stack Legal Research, free access to 12M+ legal documents.

Related

General Electric Capital Corp. v. Posey
415 F.3d 391 (Fifth Circuit, 2005)
Bell Atlantic Corp. v. Twombly
550 U.S. 544 (Supreme Court, 2007)
Ashcroft v. Iqbal
556 U.S. 662 (Supreme Court, 2009)
TROOIEN v. Mansour
608 F.3d 1020 (Eighth Circuit, 2010)
United States v. Corinthian Colleges
655 F.3d 984 (Ninth Circuit, 2011)
Richard W. Bosse v. Crowell Collier and MacMillan
565 F.2d 602 (Ninth Circuit, 1977)
James Brown v. Electronic Arts, Inc.
724 F.3d 1235 (Ninth Circuit, 2013)
Pettay v. Insurance Marketing Services, Inc.
752 P.2d 18 (Court of Appeals of Arizona, 1987)
Van Buren v. Pima Community College District Board
546 P.2d 821 (Arizona Supreme Court, 1976)
Cousins v. Lockyer
568 F.3d 1063 (Ninth Circuit, 2009)
Blank v. Talley Industries, Inc.
390 F. Supp. 1 (S.D. New York, 1975)
Neilson v. Union Bank of California, N.A.
290 F. Supp. 2d 1101 (C.D. California, 2003)
Vander Pas v. Unum Life Insurance Co. of America
7 F. Supp. 2d 1011 (E.D. Wisconsin, 1998)
Jack Carlon v. Michael E. Thaman
130 F.3d 309 (Eighth Circuit, 1997)