Peter v. STRYKER ORTHOPAEDICS, INC.

581 F. Supp. 2d 813, 2008 U.S. Dist. LEXIS 78228, 2008 WL 4491735
CourtDistrict Court, E.D. Michigan
DecidedOctober 6, 2008
DocketCase 07-13298
StatusPublished
Cited by2 cases

This text of 581 F. Supp. 2d 813 (Peter v. STRYKER ORTHOPAEDICS, INC.) is published on Counsel Stack Legal Research, covering District Court, E.D. Michigan primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Peter v. STRYKER ORTHOPAEDICS, INC., 581 F. Supp. 2d 813, 2008 U.S. Dist. LEXIS 78228, 2008 WL 4491735 (E.D. Mich. 2008).

Opinion

OPINION AND ORDER GRANTING IN PART AND DENYING IN PART DEFENDANT’S MOTION FOR PARTIAL SUMMARY JUDGMENT

PATRICK J. DUGGAN, District Judge.

On July 3, 2007, Plaintiff James Peter filed this lawsuit in Wayne County Circuit Court, against Defendants Stryker Ortho-paedics, Inc., The Stryker Corporation, Stryker Biotech, L.L.C., Howmedica Os-teonics Corp., and Stryker Technologies Corp. Plaintiff alleged three claims: statutory products liability, breach of warranty, and a violation of the Michigan Consumer Protection Act (“MCPA”), Mich. Comp. Laws § 445.903(1), stemming from injuries he suffered from a prosthetic knee designed, manufactured, and sold by Defendants. Presently before this Court is Defendant Howmedica Osteonics Corp.’s motion for partial summary judgment on Plaintiffs MCPA and statutory products liability claims. Defendant’s motion has been fully briefed, and this Court held a motion hearing on August 20, 2008. For the reasons set forth below, the Court grants in part and denies in part Defendant’s motion for partial summary judgment.

I. Facts and Procedural Background

After nearly two decades of right knee problems, Plaintiff underwent total knee replacement surgery on June 12, 2000. At that time, Plaintiffs surgeon implanted a Howmedica Duracon Total Knee system. Thereafter, Plaintiff enjoyed a year of improved mobility and decreased pain.

Nonetheless, Plaintiffs medical records reveal that by October 2001 he was once again experiencing pain and swelling in his right knee. Despite various treatments, Plaintiff continued to have problems that his doctors attributed to chronic infection. When Plaintiffs condition failed to improve after several years, Plaintiffs doctor *815 began to speculate that the tibial component of Plaintiffs prosthetic knee might have loosened, causing the pain and swelling. In an attempt to remedy the suspected loosening, Plaintiff underwent revision surgery on July 5, 2004. At that time, Plaintiffs prosthetic knee was removed and the surgeon discovered that the tibial base plate component of the prosthesis had a “definite fracture.” The fractured plate had damaged the surface of the bone requiring that the bone be shaved down four to five millimeters before a new prosthesis could be implanted. Plaintiff has continued to experience knee problems since the July 2004 surgery.

Plaintiff brought the present suit in state court on July 3, 2007, alleging that some of the prosthetic components of his Howmedica Duracon Total Knee system were defective and failed prematurely after implantation. On August 8, 2007, defendants removed Plaintiffs complaint to this Court pursuant to 28 U.S.C. § 1441. On September 13, 2007, the parties stipulated to the dismissal of all of the defendants except for Howmedica Osteonics Corp. (“Defendant”). Defendant brought the present motion for partial summary judgment pursuant to Federal Rule of Civil Procedure 56(c) on June 20, 2008.

II. Standard for Summary Judgment

Summary judgment is appropriate only when there is no genuine issue as to any material fact and the moving party is entitled to judgment as a matter of law. See Fed.R.Civ.P. 56(c). The central inquiry is “whether the evidence presents a sufficient disagreement to require submission to a jury or whether it is so one-sided that one party must prevail as a matter of law.” Anderson v. Liberty Lobby, Inc., 477 U.S. 242, 251-52, 106 S.Ct. 2505, 2512, 91 L.Ed.2d 202 (1986). After adequate time for discovery and upon motion, Rule 56(c) mandates summary judgment against a party who fails to establish the existence of an element essential to that party’s case and on which that party bears the burden of proof at trial. See Celotex Corp. v. Catrett, 477 U.S. 317, 322, 106 S.Ct. 2548, 2552, 91 L.Ed.2d 265 (1986). The movant has an initial burden of showing “the absence of a genuine issue of material fact.” Id. at 323, 106 S.Ct. at 2553. Once the movant meets this burden, the non-movant must come forward with specific facts showing that there is a genuine issue for trial. Matsushita Electric Indus. Co. v. Zenith Radio Corp., 475 U.S. 574, 587, 106 S.Ct. 1348, 1356, 89 L.Ed.2d 538 (1986). To demonstrate a genuine issue, the non-movant must present sufficient evidence upon which a jury could reasonably find for the non-movant; a “scintilla of evidence” is insufficient. Liberty Lobby, 477 U.S. at 252, 106 S.Ct. at 2512.

The court must accept as true the non-movant’s evidence and draw “all justifiable inferences” in the non-movant’s favor. Id. at 255, 106 S.Ct. at 2513. The inquiry is whether the evidence presented is such that a jury applying the relevant evidentia-ry standard could “reasonably find for either the plaintiff or the defendant.” Id. at 255, 106 S.Ct. at 2514.

III. Plaintiffs MCPA Claim

Defendant seeks summary judgment on Plaintiffs MCPA claim, arguing that the transaction or conduct at issue, i.e., sale of the prosthetic knee was regulated by the Food and Drug Administration (“FDA”) and, therefore, cannot form the basis of a MCPA claim.

The MCPA protects Michigan consumers from “unfair, unconscionable, or deceptive methods, acts, or practices in the conduct of trade or commerce.” Mich. Comp. Laws § 445.903(1). Plaintiff claims that Defendant failed to provide the promised benefits of the prosthetic knee to him in violation of section (y) of the MCPA. *816 Mich. Comp. Laws § 445.903(l)(y). Mich. Comp. Laws § 445.904(l)(a) provides that the MCPA does not apply to “[a] transaction or conduct specifically authorized under laws administered by a regulatory board or officer acting under statutory authority of this state or the United States.” The Michigan Supreme Court has held that, in determining if a transaction or conduct is exempt from the scope of the MCPA, “the relevant inquiry is not whether the specific misconduct alleged by the plaintiffs is ‘specifically authorized.’ Rather, it is whether the general transaction is specifically authorized by law, regardless of whether the specific misconduct alleged is prohibited.” Smith v. Globe Life Ins. Co., 460 Mich. 446, 465, 597 N.W.2d 28, 38 (1999).

Here, the specific misconduct Plaintiff complains of is Defendant’s “failure to provide the promised benefits in connection-ion [sic] with the transaction at issue.” (Compl. ¶ 30.) The general transaction, however, is the sale of the prosthetic knee. Prosthetic knees are medical devices, which are heavily regulated by the FDA. 21 C.F.R.

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Bluebook (online)
581 F. Supp. 2d 813, 2008 U.S. Dist. LEXIS 78228, 2008 WL 4491735, Counsel Stack Legal Research, https://law.counselstack.com/opinion/peter-v-stryker-orthopaedics-inc-mied-2008.