Montgomery v. Wyeth

540 F. Supp. 2d 933, 2008 U.S. Dist. LEXIS 23591, 2008 WL 747147
CourtDistrict Court, E.D. Tennessee
DecidedMarch 19, 2008
Docket1:05-cv-323
StatusPublished
Cited by8 cases

This text of 540 F. Supp. 2d 933 (Montgomery v. Wyeth) is published on Counsel Stack Legal Research, covering District Court, E.D. Tennessee primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Montgomery v. Wyeth, 540 F. Supp. 2d 933, 2008 U.S. Dist. LEXIS 23591, 2008 WL 747147 (E.D. Tenn. 2008).

Opinion

MEMORANDUM

CURTIS L. COLLIER, Chief Judge.

Rarely does this Court suggest that a legislative body reconsider one of its enactments. The Court believes its role is simply to apply the law applicable to the case before it and not concern itself with the merits of the case. However, because of the result in this case, this is one of those rare cases where the Court believes it is appropriate to urge the Tennessee legislature to look closely at the law governing this case.

Plaintiff Angela Montgomery (“Plaintiff’) alleges she used the diet drug Pondi-min in 1996 and 1997. According to Plaintiff, Pondimin caused her to develop Primary Pulmonary Hypertension, a progressive, fatal disease, in 2005. Later that year, she filed this product liability ease against Pondimin’s manufacturer, defendant Wyeth (“Defendant”). 1 Invoking a rarely-used provision in Tennessee’s product liability statute of repose, Defendant moved for summary judgment, claiming Plaintiffs case was untimely (Court File Nos. 83). The Court has considered the briefs filed by Defendant (Court File Nos. 84, 101 & 107) and Plaintiff (Court File Nos. 98 & 106). As explained below, the statute of repose eliminated Plaintiffs cause of action before it accrued, and therefore Defendant’s motion for summary judgment will be GRANTED (Court File No. 83).

I. BACKGROUND

Plaintiff was an overweight but healthy woman when she began taking Pondimin, a diet drug manufactured, licensed, marketed, and detailed by Defendant. She took Pondimin for over 90 days in 1996 and 1997. Pondimin, which was made from a combination therapy of fenfluramine and phentermine, known as “Fenphen,” was withdrawn from the market in September 1997, and the Food and Drug Administration found it to be unsafe.

In 2005, Plaintiff was diagnosed with Primary Pulmonary Hypertension (“PPH”), a rare, progressive, debilitating, and fatal disease affecting the heart and lungs. She alleges Pondimin caused her to develop PPH. Defendant allegedly knew of the dangers of Pondimin since at least 1995 but downplayed and concealed evidence of serious side effects and opposed putting prominent black box warnings on the drug. Plaintiff contends it is widely accepted Pondimin causes PPH, including latent PPH. Defendant does not deny Pon-dimin can cause PPH, but denies it caused PPH in Plaintiff.

Plaintiff filed this case in state court in October 2005, and it was removed to this Court in November 2005 (Court File No. 1). The ease was transferred to a Multi-District Litigation (“MDL”) court for pretrial proceedings in February 2006 (Court File No. 11) and remanded to this Court in *937 July 2007 (Court File No. 14). After the parties had fully briefed Daubert motions regarding expert witnesses, Defendant filed its summary judgment motion.

II. STANDARD OF REVIEW

Summary judgment is proper when “the pleadings, the discovery and disclosure materials on file, and any affidavits show that there is no genuine issue as to any material fact and that the movant is entitled to judgment as a matter of law.” Fed.R.Civ.P. 56(c).

First, the moving party must demonstrate no genuine issue of material fact exists. Celotex Corp. v. Catrett, 477 U.S. 317, 323, 106 S.Ct. 2548, 91 L.Ed.2d 265 (1986); Leary v. Daeschner, 349 F.3d 888, 897 (6th Cir.2003). The Court views the evidence, including all reasonable inferences, in the light most favorable to the non-movant. Matsushita Elec. Indus. Co., Ltd. v. Zenith Radio Corp., 475 U.S. 574, 106 S.Ct. 1348, 89 L.Ed.2d 538 (1986); Nat’l Satellite Sports, Inc. v. Eliadis Inc., 253 F.3d 900, 907 (6th Cir.2001). However, the non-movant is not entitled to a trial based solely on its allegations, but must submit significant probative evidence to support its claims. Celotex, 477 U.S. at 324, 106 S.Ct. 2548; McLean v. Ontario, Ltd., 224 F.3d 797, 800 (6th Cir.2000). The moving party is entitled to summary judgment if the non-movant fails to make a sufficient showing on an essential element for which it bears the burden of proof. Celotex, 477 U.S. at 323, 106 S.Ct. 2548. In short, if the Court concludes a fair-minded jury could not return a verdict in favor of the non-movant based on the record, the Court may enter summary judgment. Anderson v. Liberty Lobby, Inc., 477 U.S. 242, 251-52, 106 S.Ct. 2505, 91 L.Ed.2d 202 (1986); Lansing Dairy, Inc. v. Espy, 39 F.3d 1339, 1347 (6th Cir.1994).

III. DISCUSSION

A. The Product Liability Statute of Repose

Defendant contends Plaintiffs complaint is barred by Tennessee’s product liability statute of repose. Plaintiffs case is based on personal injury resulting from a product, and therefore is a product liability action as defined in the product liability statute, Tenn.Code Ann. § 29-28-102(6). The product liability statute of repose states:

Any action against a manufacturer or seller of a product for injury to person or property caused by its defective or unreasonably dangerous condition must be brought within the period fixed by §§ 28-3-104 [etc.], but notwithstanding any exceptions to these provisions, it must be brought within six (6) years of the date of injury, in any event, the action must be brought within ten (10) years from the date on which the product was first purchased for use or consumption, or within one (1) year after the expiration of the anticipated life of the product, whichever is the shorter

§ 29-28-103 (emphasis added). The “anticipated life of the product” is the “expiration date placed on the product by the manufacturer when required by law but shall not commence until the date the product was first purchased for use or consumption.” § 29-28-102. 2

*938 Defendant stopped manufacturing Pon-dimin on September 2, 1997 (Court File Nos. 84-4, p. 2 & 84-6). Defendant’s evidence establishes that the packaging for Pondimin contained expiration dates as required by law, and those expiration dates were three years from the date of manufacture (Court File No. 84-4 p. 2); 21 C.F.R 201.17; 21 C.F.R.

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Cite This Page — Counsel Stack

Bluebook (online)
540 F. Supp. 2d 933, 2008 U.S. Dist. LEXIS 23591, 2008 WL 747147, Counsel Stack Legal Research, https://law.counselstack.com/opinion/montgomery-v-wyeth-tned-2008.