Gregory Kline v. Zimmer Holdings IncGregory Kline v. Zimmer Holdings Inc
Here, the Cargilles alleged in the Joint Notice of Removal that they and Green Tree are citizens of different states and that the amount in controversy exceeds $75,000 based on the amount of their note and the value of the property. See
Green Tree states, similar to the District Court, that the Cargilles referred to
Accordingly, because the District Court was precluded by statute from remanding the foreclosure action on a non-jurisdictional ground, we will vacate the District Court‘s order granting the motion to remand and denying the motion to dismiss as moot.
Adrienne F. Busby, Esq., Patrick H. Reilly, Esq., Jane D. Wilson, Esq., Faegre Baker & Daniels, Indianapolis, IN, Mindy A. Finnigan, Esq., Faegre Baker Daniels, Chicago, IL, Mark E. Gebauer, Esq., Eckert Seamans Cherin & Mellott, Harrisburg, PA, Carolyn B. McGee, Esq., William T. Polaski, Esq., Amy J. Roy, Esq., Eckert Seamans Cherin & Mellott, Pittsburgh, PA, for Defendant-Appellee
Before: AMBRO, SMITH *, and FISHER, Circuit Judges
OPINION **
SMITH, Circuit Judge.
On January 13, 2010, Gregory Kline underwent a total hip replacement. His surgeon implanted a Femoral Stem with Kinectiv Technology. On April 6, 2011, Kline‘s hip replacement broke; the stem fractured at the neck. Kline sued Zimmer Holdings Inc., Zimmer Inc., and Zimmer United States Inc. (collectively, “Zimmer“), alleging several state-law product liability claims. By the time the case reached summary judgment, Kline‘s only remaining claims were negligent design defect and negligent failure to warn.1 The District Court granted summary judgment to Zimmer on all counts. Because Kline failed to show that a reasonable jury could find that
any unreasonable act or omission by Zimmer caused him harm, we will affirm the judgment of the District Court.
The District Court had jurisdiction under
We review the District Court‘s disposition of a summary judgment motion de novo, applying the same standard, as the District Court. Doe v. Luzerne County, 660 F.3d 169, 174 (3d Cir. 2011). “[W]hen the nonmoving party is the plaintiff, he must produce sufficient evidence to establish every element that he will be required to prove at trial.” J.S. ex rel. Snyder v. Blue Mountain Sch. Dist., 650 F.3d 915, 925 (3d Cir. 2011) (en banc).
Under Pennsylvania law, a plaintiff must show four elements to establish a negligence claim: duty, breach, causation, and damages. See Phillips v. Cricket Lighters, 576 Pa. 644, 841 A.2d 1000, 1008 (2003); Morena v. S. Hills Health Sys., 501 Pa. 634, 462 A.2d 680, 684 n.5 (1983). Demonstrating breach requires showing that the defendant acted unreasonably. See, e.g., Phillips, 841 A.2d at 1008 (holding that negligence claims require an inquiry “into the reasonableness of the manufacturer‘s conduct in creating and distributing such a product“). Reasonableness requires comparing the risk and the utility of the alleged acts or omissions. See, e.g., Benson v. Penn Cent. Transp. Co., 463 Pa. 37, 342 A.2d 393, 397 (1975) (“A risk is unreason-
Thus, to survive summary judgment, Kline has to show that there is a genuine issue of material fact that Zimmer acted unreasonably in designing the stem or failing to warn about the stem and that any unreasonable act was the cause of the harm to Kline. Kline failed to do so.2
On appeal, Kline primarily contends the District Court erred because the District Court did not fully consider two affidavits filed after the Magistrate Judge first recommended granting Zimmer‘s summary judgment motion. Because these affidavits do not advance Kline‘s reasonableness or design causation arguments, they do not affect summary judgment. Therefore, this Court need not address Kline‘s arguments that the sham affidavit doctrine was improperly applied3 or that certain portions of the affidavit of Klein‘s surgeon were admissible.
Kline argues that the failure of the Zimmer device in another patient treated by Kline‘s doctor—an issue raised in both affidavits—is important here. Evidence about the other patient‘s device failure is not admissible, however, because it did not “involv[e] the same product under similar circumstances,” nor did it (1) “show notice to the defendant of the danger,” (2) “show [the] existence of the danger,” or (3) “show the cause of the accident.” Gumbs v. Int‘l Harvester, Inc., 718 F.2d 88, 97 (3d Cir. 1983). Here, the other patient‘s device failure could not show notice of the danger because the allegedly related device failure occurred after the Zimmer device already had been implanted in Kline. The other patient‘s device failure also does not prove the “existence of the danger” or “cause of the accident” because Kline fails to offer any sort of causation theory regarding the prior accident—let alone one related to any unreasonable act that affected his own device. There is no reason to believe that whatever latent danger allegedly harmed the other patient had any relationship to Kline. Kline‘s lack of a causation theory for the other patient‘s device failure means Kline failed to show that there were relevant “similar circumstances.” Gumbs, 718 F.2d at 97.
With regard to the negligent design defect claim, the District Court held that Plaintiffs’ experts, Mari Truman and Dr. Donald Koss, had waived Kline‘s design defect claims in their depositions.
Kline failed to produce record evidence showing any of these design choices were unreasonable, thus causing his device to fail. With regard to unreasonableness, Kline failed to provide record evidence from which a jury could find that the allegedly faulty design changes increased risk more than they increased utility. See Metzgar, 30 F.3d at 462 (conducting risk-utility analysis in a negligent design case), See generally Tincher v. Omega Flex, Inc., 628 Pa. 296, 104 A.3d 328, 389-91 (2014) (discussing risk-utility analysis). Instead, for instance, Truman refers to a “NEW and foreseeable risk.” Whether a new risk is unreasonable can only be determined based on a comparison with alternative risks and benefits, cf. Peter Huber, Safety and the Second Best: The Hazards of Public Risk Management in the Courts, 85 Colum. L. Rev. 277, 309 (1985) (“[T]he rejection of one risk is always the acceptance of another.“), or proof that the new risk was of such magnitude and likelihood that it was facially unreasonable, see Lance v. Wyeth, 624 Pa. 231, 85 A.3d 434, 458-59, 458 n.36 (2014) (discussing the common use of an alternative design and approving plaintiff‘s theory that defendant “tender[ed] into the market a drug which it knows or should know is so dangerous that it should not be taken by anyone“). Here, there is neither sufficient record evidence about the relative risks of an alternative design nor sufficient record evidence that the stem is so dangerous that a jury could find Zimmer‘s design choices were unreasonable.
Moreover, to the extent Kline presented admissible causation evidence, that evidence does not support any of Kline‘s theories of unreasonable design. For example, Truman failed to show how increased testing would have resulted in a design change; Truman admitted that she did not have “information” to conclude that different surface treatment would have prevented the stem fracture; and Kline‘s metallurgy expert admitted he was not aware of a better material to use for the stem.
Summary judgment also must be granted to Zimmer on Kline‘s failure to warn claim. Kline‘s theory, supported by Zimmer‘s experts, was that an individual of Kline‘s weight or body mass index who engaged in vigorous activity was at a higher risk of device failure. As Kline acknowledged, a package insert for Zimmer‘s device warned about those risks, at least in general terms.4 Truman opined that there
D. BROOKS SMITH
UNITED STATES CIRCUIT JUDGE