Allen v. Zimmer Holdings, Inc. et al, No. 3:2015cv00341 - Document 30 (D. Nev. 2015)
Court Description: ORDER denying Stryker's 7 Motion to Dismiss; granting Allen's 19 Request for Leave to Amend. Amended complaint due within 30 days. If none filed, final dismissal of this action will be entered. Signed by Judge Larry R. Hicks on 10/30/2015. (Copies have been distributed pursuant to the NEF - KR)
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Allen v. Zimmer Holdings, Inc. et al Doc. 30 1 2 3 4 5 UNITED STATES DISTRICT COURT DISTRICT OF NEVADA 6 7 *** 8 9 JACQUE ALLEN, 10 Plaintiff, 11 v. 12 13 14 15 16 17 18 3:15-CV-00341-LRH-VPC ORDER ZIMMER HOLDINGS, INC., a foreign corporation; ZIMMER, INC., a foreign corporation; ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC., a foreign corporation; STRYKER HOLDINGS, LLC, a domestic limited liability company; STRYKER CORPORATION, a foreign corporation; HOWMEDICA OSTEONICS CORP., a foreign corporation, doing business as STRYKER ORTHOPAEDICS; ABC CORPORATIONS II-X; BLACK AND WHITE COMPANIES II-X; and JOHN DOES II-X, inclusive, Defendants. 19 20 Before the Court is Defendants Stryker Corporation and Howmedica Osteonics Corp. 21 22 d/b/a Stryker Orthopaedics’ (collectively, “Stryker”) Motion to Dismiss Plaintiff Jacque Allen’s 23 (“Allen”) First Amended Complaint (“FAC”). Doc. #7.1 Allen filed an Opposition, which 24 included a request for leave to amend (Doc. #19), to which Stryker replied (Doc. #21). 25 I. Factual Background 26 This case involves strict product liability, negligence, and breach of implied and express 27 warranty claims that arose out of the implantation of an artificial hip prosthesis manufactured by 28 1 Refers to the Court’s docket number. 1 Dockets.Justia.com 1 Defendants Zimmer Holdings, Inc.; Zimmer, Inc.; and Zimmer Orthopaedic (collectively, 2 “Zimmer”) and the use of Stryker’s Surgical Simplex P Radiopaque Bone Cement (“Simplex”) 3 and Howmedica Sterile R Log Medium Bone Plug (“Bone Plug”). On or about June 17, 2008, Allen underwent hip surgery utilizing products produced by 4 5 the defendants. After benefiting from the right hip replacement for several years, Allen began 6 experiencing groin pain in late 2012. Allen consulted with her orthopedic surgeon who 7 suspected that the site of the right hip prosthesis was “loose.” On January 8, 2013, Allen was 8 seen by another orthopedic surgeon, Dr. Jackson Jones, who recommended revision of the 9 femoral component. Revision of the right total hip procedure was conducted on February 24, 10 2013. 11 On February 13, 2015, Allen filed an action in the Second Judicial District Court for the 12 State of Nevada in and for the County of Washoe. Doc. # 1 Ex. 2. She filed her First Amended 13 Complaint on June 10, 2015. Doc. #1 Ex. 1. The case was removed to federal court. On July 7, 14 2015, Stryker filed its Motion to Dismiss. Doc. #7. Allen responded on August 3, 2015. Doc. 15 #19. Stryker filed a Reply on August 7, 2015. Doc. #21. 16 II. Legal Standard 17 Stryker seeks dismissal for failure to state a claim upon which relief can be granted 18 pursuant to Federal Rule of Civil Procedure 12(b)(6). To survive a motion to dismiss for failure 19 to state a claim, a complaint must satisfy the Federal Rule of Civil Procedure 8(a)(2) notice 20 pleading standard. Mendiondo v. Centinela Hosp. Med. Ctr., 521 F.3d 1097, 1103 (9th Cir. 21 2008). That is, a complaint must contain “a short and plain statement of the claim showing that 22 the pleader is entitled to relief.” Fed. R. Civ. P. 8(a)(2). The 8(a)(2) pleading standard does not 23 require detailed factual allegations, but a pleading that offers “‘labels and conclusions’ or ‘a 24 formulaic recitation of the elements of a cause of action’” will not suffice. Ashcroft v. Iqbal, 556 25 U.S. 662, 678 (2009) (quoting Bell Atl. Corp. v. Twombly, 550 U.S. 544, 555 (2007)). 26 To satisfy the plausibility standard, 8(a)(2) requires a complaint to “contain sufficient 27 factual matter, accepted as true, to ‘state a claim to relief that is plausible on its face.’” Id. 28 (quoting Twombly, 550 U.S. at 570). A claim has facial plausibility when the pleaded factual 2 1 content allows the Court to draw the reasonable inference, based on the Court’s “judicial 2 experience and common sense,” that the defendant is liable for the misconduct alleged. See id. at 3 678-79. The plausibility standard “is not akin to a probability requirement, but it asks for more 4 than a sheer possibility that a defendant has acted unlawfully. Where a complaint pleads facts 5 that are merely consistent with a defendant’s liability, it stops short of the line between 6 possibility and plausibility of entitlement to relief.” Id. at 678 (internal quotation marks 7 omitted). 8 9 In reviewing a motion to dismiss, the court accepts the facts alleged in the complaint as true. Id. The “factual allegations that are taken as true must plausibly suggest an entitlement to 10 relief, such that it is not unfair to require the opposing party to be subjected to the expense of 11 discovery and continued litigation.” Starr v. Baca, 652 F.3d 1202, 1216 (9th Cir. 2011). 12 Moreover, “bare assertions . . . amount[ing] to nothing more than a formulaic recitation of the 13 elements of a . . . claim . . . are not entitled to an assumption of truth.” Moss v. U.S. Secret Serv., 14 572 F.3d 962, 969 (9th Cir. 2009) (citing Iqbal, 556 U.S. at 681) (brackets in original) (internal 15 quotation marks omitted). The court discounts these allegations because “they do nothing more 16 than state a legal conclusion—even if that conclusion is cast in the form of a factual allegation.” 17 Id. (citing Iqbal, 556 U.S. at 681). “In sum, for a complaint to survive a motion to dismiss, the 18 non-conclusory ‘factual content,’ and reasonable inferences from that content, must be plausibly 19 suggestive of a claim entitling the plaintiff to relief.” Id. 20 Before trial, a party can amend its complaint twenty-one days after serving it or twenty- 21 one days after service of a responsive pleading or motion to dismiss under Rule 12(b)(6). Fed. 22 R. Civ. P. 15(a)(1). The court can also grant leave to amend “when justice so requires.” Fed. R. 23 Civ. P. 15(a)(2). If the court grants a motion to dismiss, “[t]he standard for granting leave to 24 amend is generous.” Balistreri v. Pacifica Police Dep’t, 901 F.2d 696, 701 (9th Cir. 1990). The 25 Court will generally only decline to grant leave to amend if the party opposing amendment 26 shows “bad faith, undue delay, prejudice to the opposing party, futility of amendment,” or that 27 the plaintiff has previously amended the complaint without healing its defects. United States v. 28 3 1 Corinthian Colls., 655 F.3d 984, 995 (9th Cir. 2011) (citing Johnson v. Buckley, 356 F.3d 1067, 2 1077 (9th Cir. 2004)). 3 III. Discussion 4 5 A. Premarket Approval and Federal Preemption a. Premarket Approval 6 Stryker argues that Allen’s claims are preempted by the Medical Device Amendments 7 (“MDA”) of 1976 to the Federal Drug and Cosmetic Act. The MDA grants the Federal Drug 8 Administration (“FDA”) regulatory authority over medical devices and defines three tiers of 9 regulation. 21 U.S.C. § 360c. The three regulatory tiers correspond to the inherent risk of using 10 the device, with Class III representing the greatest level of risk. See Riegel v. Medtronic, Inc., 11 552 U.S. 312, 128 S.Ct. 999, 1003, 169 L.Ed.2d 892 (2008). Developers of new Class III 12 devices are required to obtain premarket approval (“PMA”), the FDA's highest level of 13 oversight. Id. at 1003–1004, 21 U.S.C. § 360c(a)(1)(C). Simplex, one of the products at issue 14 here, was developed prior to the MDA and went through the FDA’s New Drug Application 15 (“NDA”) process. When the MDA came into effect, devices such as Simplex, which had been 16 treated as drugs prior to the amendments to the 1938 Act, were automatically reclassified as 17 Class III medical devices. See 21 U.S.C. § 360j(l )(1). The MDA provided that these devices 18 were deemed to have PMA approval if they had gone through the NDA approval process. Id. at 19 § 360j(l )(3)(A). Beginning in 1976 Simplex was accordingly treated as a Class III medical 20 device with PMA approval. 21 In 2002, the FDA re-classified Simplex as a Class II medical device. This change does 22 not affect the analysis here because preemption analysis focuses on how the product came to 23 market, not its current classification. In re Medtronic, Inc. Sprint Fidelis Leads Products Liab. 24 Litig., 592 F. Supp. 2d 1147, 1156 (D. Minn. 2009) aff'd sub nom. In re Medtronic, Inc., Sprint 25 Fidelis Leads Products Liab. Litig., 623 F.3d 1200 (8th Cir. 2010) and aff'd sub nom. In re 26 Medtronic, Inc., Sprint Fidelis Leads Products Liab. Litig., 623 F.3d 1200 (8th Cir. 2010) 27 “[P]reemption necessarily looks backward (to the time of PMA) rather than forward” because 28 retroactive second-guessing on the FDA’s decision-making would interfere with the PMA 4 1 process. Id. Thus, Simplex is still treated as having PMA approval for the purposes of MDA 2 preemption analysis. 3 Additionally, the Bone Plug used with Simplex is considered to have been approved 4 through the PMA process. Component parts, like the Bone Plug, are considered to have the 5 same PMA approval as the device of which they are a component. Cornwell v. Stryker Corp., 6 2010 WL 4641112 (D. Idaho Nov. 1, 2010); Lewkut v. Stryker Corp., 724 F. Supp. 2d 648, 656 7 (S.D. Tex. 2010); Riley v. Cordis Corp. 625 F. Supp. 2d 769, 779-80 (D. Minn. 2009). Thus 8 both Simplex and the Bone Plug are considered to have PMA approval for the purposes of MDA 9 preemption analysis. 10 11 12 b. Federal Preemption Along with providing a regulatory framework for medical devices, Congress included a preemption clause in the MDA that states: 13 [N]o State or political subdivision of a State may establish or continue in effect 14 with respect to a device intended for human use any requirement— 15 (1) which is different from, or in addition to, any requirement applicable under 16 17 18 19 this chapter to the device, and (2) which relates to the safety or effectiveness of the device or to any other matter included in a requirement applicable to the device under this chapter. 21 U.S.C. § 360k(a). 20 In Riegel, the Supreme Court held § 360k(a) preempts a number of common law claims 21 stemming from the failure of a Class III device. Riegel, 552 U.S. at 321. The Court established 22 a two-pronged test for claim preemption under § 360k(a). Id. First, courts must determine if the 23 federal government has established requirements relating to the device. Id. If so, courts then 24 evaluate whether a state claim imposes requirements relating to the safety and effectiveness of 25 the device that are “different from, or additional to,” federal requirements. Id. 26 The Supreme Court held that the FDA's premarket approval process “imposes 27 requirements under the MDA” for Class III devices, satisfying the first prong of the test. Id. at 28 1007 (internal quotations omitted). Therefore, it is the second prong of the Riegel test that is 5 1 often determinative; specifically, whether the claims relate to the safety and effectiveness of the 2 device. Horn v. Boston Scientific Neuromodulation Corp., No. CV409-074, 2011 WL 3893812, 3 at *4 (S.D. Ga. Aug. 26, 2011. In Riegel, the Court concluded that common law claims for 4 negligence, strict liability, and breach of implied warranty are examples of state law 5 “requirements” that relate to the safety or effectiveness of a device, and are thus preempted. 6 Riegel, 552 U.S. at 322-26. This is because “[s]tate tort law that requires a [device] to be safer, 7 but hence less effective, than the model the FDA has approved disrupts the federal scheme,” and 8 is preempted. Id. at 1008. 9 Additionally, Riegel also introduced the concept of “parallel claims,” which provide a 10 narrow exception to MDA preemption. Riegel, 552 U.S. at 329. The Court explained that state 11 claims based on a violation of FDA regulations are not preempted under the MDA. Id. The 12 Court reasoned that “[s]tate requirements are pre-empted under the MDA only to the extent that 13 they are ‘different from, or in addition to,’ the requirements imposed by federal law.” Id. 14 (quoting § 360k(a)(1)). Thus, purposely pled state claims based on violations of FDA 15 regulations are not preempted by § 360k(a), as those claims do not conflict with, but rather 16 parallel, the statutory scheme. Id. ‘To properly plead parallel claims that survive preemption, a 17 plaintiff must allege facts (1) showing an alleged violation of FDA regulations or requirements 18 related to [the device], and (2) establishing a causal nexus between the alleged injury and the 19 violation.’” Martin v. Medtronic, Inc., 32 F. Supp. 3d 1026, 1034 (D. Ariz. 2014) (quoting 20 Eidson v. Medtronic, Inc., ––– F.Supp.3d ––––, ––––, 2014 WL 1996024, at *7 (N.D.Cal.2014)). 21 The question of whether MDA preemption applies to claims involving the breach of 22 express warranties has not been decided by the Supreme Court. Courts have held claims for 23 breach of express warranty to be preempted primarily where the warranty directly relates to the 24 safety or effectiveness of the device. See Leonard v. Medtronic, Inc., No. 1:10-CV-03787-JEC, 25 2011 WL 3652311, at *10 (N.D. Ga. Aug. 19, 2011) (holding that a claim for breach of express 26 warranty that a device was “safe and highly reliable” would conflict with the FDA's conclusion 27 the device was “reasonably safe and effective” and is thus preempted); In re Medtronic, Inc., 592 28 F.Supp.2d 1147, 1164 (D. Minn. 2009) (holding that claims for breach of an express warranty of 6 1 a medical device's safety would require a jury to determine that the device was unsafe); Miller v. 2 DePuy Spine, Inc., 638 F.Supp.2d 1226, 1230 (D. Nev. 2009) (holding that a breach of express 3 warranty claim was preempted where an essential element of the claim includes “proof that a 4 device granted a [PMA] is not safe or effective”). This differs from something like a voluntarily 5 imposed limited warranty guaranteeing craftsmanship, a type of express warranty some courts 6 have found not to be preempted. Cline v. Advanced Neuromodulation Sys., Inc., 914 F. Supp. 2d 7 1290, 1298 (N.D. Ga. 2012); Horn, 2011 WL 3893812, at *. 8 9 Allen’s complaint does not contain adequate allegations to survive MDA preemption. Because the products at issue are deemed to have PMA approval, requirements are imposed 10 under the MDA, and the first prong of the Riegel test is met; however, Allen fails at the second 11 prong. To satisfy the second prong, the state claims must impose requirements relating to safety 12 and effectiveness that are different from or additional to the federal requirements. Here, Allen’s 13 product liability, negligence, and implied warranty claims are based on the safety and 14 effectiveness of the Simplex and Bone Plug, and thus are preempted by the MDA. Nothing in 15 Allen’s complaint indicates her state claims are based on anything different from, or additional 16 to, the federal requirements. Allen instead relies on general claims based on common law duties 17 challenging the safety and effectiveness of Simplex and the Bone Plug. Allen makes no 18 arguments and provides no information as to how her claims parallel federal requirements or 19 how she might fit into this narrow exception. None of her claims even mention FDA regulations, 20 much less show an alleged violation of FDA regulations or establish a causal nexus between the 21 injury and the violation. Additionally, Allen’s express warranty claim also seems to be premised 22 on the general safety and effectiveness of the Simplex and Bone Plug, as opposed to something 23 like the limited craftsmanship warranties found in Cline and Horn, and would thus be preempted, 24 as well. Therefore, Allen does not demonstrate a claim that is not preempted by the MDA. 25 However, the Court will grant Allen’s request for leave to amend her complaint. 26 B. Statute of Limitations 27 Stryker argues that Allen’s claims are barred by the statute of limitations even if they 28 were tolled because the two year period would have expired at the latest in January of 2015, two 7 1 years after revision surgery was recommended. Allen does not dispute the two year statute of 2 limitations but counters that the finder of fact should determine the applicable statute of 3 limitations period for a given case. 4 NRS 11.190(4)(e) provides a two-year statute of limitations for “an action to recover 5 damages for injuries to a person or for the death of a person caused by the wrongful act or 6 neglect of another.” This applies whether the claim is articulated as negligence, breach of 7 contract, tort, or product liability. Sparks v. Alpha TauOmega Fraternity, Inc., 127 Nev ––––, –– 8 ––, n. 4, 255 P.3d 238, 243 n. 4 (2011) (applying NRS 11.190(4)(e) to a negligence personal 9 injury claim); Meadows v. Sheldon Pollack Corp., 92 Nev. 636, 637, 556 P.2d 546, 546 10 (explaining that although the plaintiff alleged breach of contract, “the gravamen of his cause of 11 action is in tort to recover damages for personal injuries; thus, the two-year limitation of NRS 12 11.190(4)(e) is applicable”); Blotzke v.Christmas Tree, Inc., 88 Nev. 449, 450, 499 P.2d 647, 647 13 (1972) (holding that a contract claim for personal injury is treated as a tort claim and the two 14 year state of limitations applies); Bender v. Clark Equipment Co. 111 Nev. 844, 897 P.2d 208, 15 208 (1995) (stating plaintiff filed his strict product liability case two days before the two-year 16 statute of limitations period had run). 17 “[A] cause of action accrues when the wrong occurs and a party sustains injuries for 18 which relief could be sought.” Petersen v. Bruen, 106 Nev. 271, 274, 792 P.2d 18, 20 (1990). 19 However, the discovery rule tolls “the statutory period of limitations ... until the injured party 20 discovers or reasonably should have discovered facts supporting a cause of action.” Id. This 21 rule requires a plaintiff to use due diligence in determining the existence of a cause of action and 22 delays the accrual of the cause of action until the plaintiff obtains inquiry notice. Bemis v. Estate 23 of Bemis, 114 Nev. 1021, 1025, 967 P.2d 437, 440 (1998). Inquiry notice occurs when a plaintiff 24 “should have known of facts that ‘would lead an ordinarily prudent person to investigate the 25 matter further.’” Winn v. Sunrise Hosp. & Med. Ctr., 128 Nev. ––––, ––––, 277 P.3d 458, 462 26 (2012) (quoting Black's Law Dictionary 1165 (9th ed. 2009)). Factual knowledge “need not 27 pertain to precise legal theories the plaintiff may ultimately pursue, but merely to the plaintiff's 28 general belief that someone's negligence may have caused his or her injury.” Id. Moreover, 8 1 “[d]ismissal on statute of limitations grounds is only appropriate ‘when uncontroverted evidence 2 irrefutably demonstrates plaintiff discovered or should have discovered’ the facts giving rise to 3 the cause of action.” Bemis, 114 Nev. at 1025, 967 P.2d at 440 (quoting Nevada Power Co. v. 4 Monsanto Co., 955 F.2d 1304, 1307 (9th Cir.1992)). 5 Here, the fact that Allen’s orthopedic surgeons suspected the right hip prosthesis was 6 loose and recommended revision surgery simply does not rise to the high level of 7 “uncontroverted evidence” irrefutably demonstrating Allen should have discovered the facts 8 giving rise to her cause of action. Because there was no irrefutable evidence that Allen was on 9 inquiry notice, this Court declines to dismiss her complaint on statute of limitations grounds. 10 IV. Conclusion 11 IT IS THEREFORE ORDERED that Stryker’s Motion to Dismiss (Doc. #7) is DENIED. 12 IT IS FURTHER ORDERED that Allen’s request for leave to amend (Doc. #19) is 13 GRANTED. If Allen chooses to file an amended complaint, such complaint shall be filed 14 within thirty (30) days of the entry of this order. 15 16 IT IS FURTHER ORDERED that if no amended complaint is filed within the thirty (30) days allotted, the Clerk of the Court shall enter the final dismissal of this action. 17 IT IS SO ORDERED. 18 DATED this 30th day of October 2015. 19 20 LARRY R. HICKS UNITED STATES DISTRICT JUDGE 21 22 23 24 25 26 27 28 9
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