Casey v. Wright Medical Technology Incorporated

CourtDistrict Court, D. Arizona
DecidedFebruary 13, 2020
Docket2:19-cv-05360
StatusUnknown

This text of Casey v. Wright Medical Technology Incorporated (Casey v. Wright Medical Technology Incorporated) is published on Counsel Stack Legal Research, covering District Court, D. Arizona primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

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

Opinion

1 WO 2

6 IN THE UNITED STATES DISTRICT COURT 7 FOR THE DISTRICT OF ARIZONA 8

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

10 Plaintiff, 11 v. ORDER 12 Wright Medical Technology, Inc., a foreign 13 corporation,

14 Defendant. 15

16 Before the Court is Defendant Wright Medical Technology, Inc.’s (“Wright”) 17 Partial Motion to Dismiss (Doc. 11). For the reasons stated below, the motion shall be 18 granted in part and denied in part. 19 I. BACKGROUND 20 The following allegations from Plaintiff Theresa I. Casey’s (“Casey”) First 21 Amended Complaint (Docs. 7, 7-1, and 7-2) are presumed true at this stage. See Brown v. 22 Elec. Arts, Inc., 724 F.3d 1235, 1247 (9th Cir. 2013) (“[O]n a motion to dismiss, the court 23 presumes that the facts alleged by the plaintiff are true.”).1 24 On August 18, 2008, Casey underwent a total hip arthroplasty (more commonly 25 known as hip replacement surgery), during which Dr. Dwight S. Keller, M.D. (“Doctor 26

27 1 Unless otherwise indicated, in citing cases, all internal quotation marks, citations, 28 emphases, alterations, and footnotes are omitted. 1 Keller”) implanted in Casey’s right hip a variety of artificial hip devices designed, 2 manufactured, distributed, sold, and marketed by Wright, including the product at issue 3 here, the “Wright Profemur® Plasma Z Stem” and its neck. (Docs. 7, 7.1, and 7.2 at ¶¶ 5, 4 7-8, 69.) A little over a year later, after Casey began experiencing pain in her right hip, Dr. 5 Keller conducted a total hip arthroplasty revision, during which he found the Wright 6 artificial hip had dislocated and again implanted a variety of Wright artificial hip devices. 7 (Id. at ¶¶ 71-73.) This procedure did not put an end to Casey’s troubles, as she had to 8 undergo a second total hip arthroplasty revision in December 2011 due to another 9 breakdown of the Wright artificial hip. (Id. at ¶¶ 75-76.) She underwent a third such 10 surgery in November 2017 after the Wright artificial hip again failed. (Id. at ¶¶ 88-89.) 11 Wright’s titanium Profemur® system is a modular hip stem and neck system. (Id. 12 at ¶ 35.) The modular stem has a separate neck component that attaches to the top of the 13 stem and a femoral ball which in turn attaches to the modular neck. (Id. at ¶¶ 37, 39-40.) 14 According to Wright, “[n]o existing hip implant is better suited to address . . . the historical 15 challenges of total hip arthroplasty.” (Id. at ¶ 41.) 16 In marketing the Profemur® system in 2008, 2009, and 2011 to Casey, Dr. Keller, 17 and the consuming public, Wright stated: “[t]he clinical effectiveness and dependability of 18 the modular necks has been consistently demonstrated throughout the PROFEMUR® Hip 19 clinical history. Utilized in both primary and revision applications, the current neck design 20 has been successfully employed to improve surgical outcomes with no reported failures.” 21 (Id. at ¶¶ 42, 125.) Touting the strength of the coupling between the neck and the stem, 22 Wright further indicated:

23 Modular neck clinical experience and extensive laboratory tests have 24 proven the coupling between the modular neck and femoral implant provides: 25

26 • Structural reliability • Absence of significant micromovement 27 • Absence of fretting corrosion 28 These excellent characteristics are obtained due to the patented geometry of 1 the coupling. The necks are made from titanium alloy (Ti6Al4V) which is 2 proven to afford suitable mechanical properties, ideal biocompatibility, and excellent resistance to corrosion. 3

4 (Id. at ¶¶ 43, 125.) 5 However, Wright “did not test the Profemur® Plasma Z system for safety before its 6 release to the public.” (Id. at ¶ 48.) Indeed, Wright marketed the system “as having a 7 clinical history of being safe on account of the clinical history of predicate devices, not the 8 actual device being marketed” and knew “there was no clinical evidence to support its 9 contention that its device was safe or effective.” (Id. at ¶¶ 51-52.) On the contrary, “[t]he 10 testing done to the product prior to the launch was woefully inadequate, unreasonable, and 11 not representative of real-world, clinical situations.” (Id. at ¶ 50.) 12 As it turned out, the Profemur® Plasma Z system was not the Wright stuff. The 13 system’s titanium alloy modular neck was prone to fretting and corrosion, which in turn 14 made it susceptible to fracture. (Id. at ¶¶ 53-55.) By 2008, Wright received a large number 15 of reports and warnings from surgeons and others regarding the Profemur® Plasma Z 16 system components and until 2009, the system experienced a high rate of failures 17 worldwide. (Id. at ¶¶ 64-65.) 18 In 2009, Wright, aware of the “high rates of problems” with the Profemur® Plasma 19 Z system, changed the design of the modular necks “from a titanium alloy to a cobalt- 20 chrome alloy in order to try to increase its safety and efficacy.” (Id. at ¶¶ 57, 61.) Yet, 21 Wright did not recall the previously-issued titanium alloy modular necks and did not issue 22 “any warning to doctors or patients who had previously received an implanted titanium 23 modular neck.” (Id. at ¶ 59.) Moreover, in 2008, 2009, and 2011, Wright did not disclose 24 information regarding the performance history, dangers, and risks of the Profemur® 25 Plasma Z system to either Casey, Dr. Keller, or the consuming public. (Id. at ¶ 122.) 26 Casey initiated this action in the Superior Court of the State of Arizona in and for 27 Maricopa County on September 18, 2019 against Wright, as well as against Wright Medical 28 Group, Inc. and numerous fictitious individuals and entities. (Doc. 1-3.) Defendants 1 timely removed the action to this Court. (Doc. 1.) On October 16, 2019, Casey filed a 2 First Amended Complaint (the “Complaint”) against Wright, which alleges four causes of 3 action: (1) Strict Product Liability—Design Defect, (2) Strict Product Liability—Failure to 4 Issue Post-Sale Warnings, (3) Negligence, and (4) Negligent Misrepresentation. (Docs. 7, 5 7-1, and 7-2.) Wright’s motion seeks an order dismissing Casey’s negligent 6 misrepresentation cause of action and prayer for punitive damages.2 7 II. ANALYSIS 8 A. Pleading Standard 9 When considering a motion to dismiss, a court evaluates the legal sufficiency of the 10 plaintiff’s pleading. Dismissal under Federal Rule of Civil Procedure (“Rule”) 12(b)(6) 11 can be based on the “lack of a cognizable legal theory” or “the absence of sufficient facts 12 alleged under a cognizable legal theory.” Balistreri v. Pacifica Police Dep’t, 901 F.2d 696, 13 699 (9th Cir. 1990). In deciding a motion to dismiss under Rule 12(b)(6), all allegations 14 of material fact are assumed to be true and construed in the light most favorable to the 15 nonmoving party. Cousins v. Lockyer, 568 F.3d 1063, 1067 (9th Cir. 2009). However, 16 this principle does not apply to legal conclusions or conclusory factual allegations. 17 Ashcroft v. Iqbal, 556 U.S. 662, 678 (2009). “Threadbare recitals of the elements of a 18 cause of action, supported by mere conclusory statements, do not suffice.” Id. Neither do 19 “naked assertion[s]” devoid of “further factual enhancement.” Bell Atl. Corp. v. Twombly, 20 550 U.S. 544, 557 (2007).

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Casey v. Wright Medical Technology Incorporated, Counsel Stack Legal Research, https://law.counselstack.com/opinion/casey-v-wright-medical-technology-incorporated-azd-2020.