Grenier v. Medical Engineering Corp.

243 F.3d 200, 2001 U.S. App. LEXIS 3466, 2001 WL 170647
CourtCourt of Appeals for the Fifth Circuit
DecidedMarch 8, 2001
Docket00-30641
StatusPublished
Cited by53 cases

This text of 243 F.3d 200 (Grenier v. Medical Engineering Corp.) is published on Counsel Stack Legal Research, covering Court of Appeals for the Fifth Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Grenier v. Medical Engineering Corp., 243 F.3d 200, 2001 U.S. App. LEXIS 3466, 2001 WL 170647 (5th Cir. 2001).

Opinion

E. GRADY JOLLY, Circuit Judge:

This appeal arises from a products liability case involving silicone gel breast implants. In March 1983, Mary Grenier received breast implants manufactured by Medical Engineering Corporation (“MEC”). Eleven years later, Grenier sued MEC after learning that silicone gel had leaked or “bled” through the implant *203 shell. The district court granted summary judgment for MEC. Grenier v. Medical Engineering Corp., 99 F.Supp.2d 759 (W.D.La.2000). The district court concluded that (1) the 1988 Louisiana Products Liability Act applied to Grenier’s claims; (2) Grenier could not prevail on her defective design and failure to warn claims because she had presented no evidence of a product defect; and (3) Grenier’s redhibition claim was time-barred. We affirm.

I

Mary Grenier underwent breast augmentation surgery following a double mastectomy in March 1983. The operating physician inserted silicone gel breast implants manufactured by MEC.

By the early 1990s, Grenier began experiencing health problems that she associated with her breast implants. In 1994, after diagnostic tests indicated that the implant in Grenier’s left breast might have ruptured, Grenier’s physician surgically removed both implants. Although the surgeon concluded that the left implant had not ruptured, he also discovered 75 to 100 cc of silicone gel outside the implant shell but within the scar tissue capsule in Grenier’s left breast. The district court and the parties refer to this phenomenon of “silicone gel passing] through the shell of the implant without any noticeable structural defect in the implant shell itself’ as “gel bleed.” Grenier, 99 F.Supp.2d at 761.

Grenier filed a complaint against MEC in the United States District Court for the Western District of Louisiana in May 1994. Grenier’s case was then transferred to the Multi-District Litigation Court (MDL-926) in the Northern District of Alabama, where it remained for four and a half year's. For reasons not relevant to this appeal, Grenier’s case was remanded to the district court in Louisiana in January 1999.

Grenier’s complaint listed fifteen theories of liability, including defective design, defective manufacture, failure to warn of the potentially dangerous nature of the product, breach of warranty, negligent misrepresentation, and redhibition. In April 2000, the district court granted MEC’s motion for summary judgment and dismissed all of Grenier’s claims. Grenier now appeals. 1

II

We review a district court’s grant of summary judgment de novo, applying the same substantive test set forth in Federal Rule of Civil Procedure 56(c). See Horton v. City of Houston, 179 F.3d 188, 191 (5th Cir.1999).

A

The first issue on appeal is whether the 1988 Louisiana Products Liability Act (“LPLA”) applies to Grenier’s claims. This question is significant to the various theories asserted by Grenier because the LPLA establishes four exclusive theories of product liability: defective design, defective manufacture, failure to warn, and breach of warranty. See La. Rev.Stat. Ann. § 9:2800.52 (West 1997)(“A claimant may not recover from a manufacturer for damage caused by a product on the basis of any theory of liability that is not set forth in the Chapter.”). The LPLA applies only to causes of action that accrued on or after September 1, 1988. Brown v. R.J. Reynolds Tobacco Co., 52 F.3d 524, 527 (5th Cir.1995). Therefore, the narrow question before us is when Grenier’s cause of action accrued.

Under Louisiana law, “A cause of action accrues when a plaintiff may bring a lawsuit. In a negligence action, for instance, the claimant must be able to allege fault, causation, and damages.” Id. at 526-27. In this case, the cause of action *204 accrued when Grenier suffered some physical injury because of her breast implants. 2

Grenier has presented no medical evidence of when her injuries may have occurred. (The only evidence remotely relevant to this question is Grenier’s testimony that she began experiencing pain in her back and shoulders sometime after 1990.) In this respect, Grenier’s case is indistinguishable from Arabie v. R.J. Reynolds Tobacco Co., 698 So.2d 423, 425 (La.App. 5 Cir.1997), in which a smoker, who was diagnosed with lung cancer in 1992, presented no evidence as to when the damage to his lungs began. A Louisiana appeals court held that the LPLA was the plaintiffs exclusive remedy because he had “failed to introduce a single piece of evidence” supporting his claim that his lung damage occurred prior to 1988. Id. Similarly, Grenier has introduced no evidence — and certainly no medical expert testimony — indicating that she suffered any injury prior to September 1988, when the LPLA took effect.

Grenier, relying exclusively on Cole v. Celotex Corp., 599 So.2d 1058 (La.1992), argues that her cause of action accrued in March 1983, when she received the breast implants. But Cole is not relevant to the issue before us. Cole involved a comparative fault statute that applied to “claims arising from events that occurred” after August 1980. The Louisiana Supreme Court explained that in long-latency occupational disease cases, the “events” contemplated by the statute would include “repeated tortious exposures” to asbestos or other disease-causing agents. Id. at 1066. Because the plaintiffs in Cole were exposed to asbestos before August 1980, the comparative fault statute did not apply. But, as the Louisiana Supreme Court recently observed, the holding in Cole “turned on [the] unique language” of the comparative fault statute. Walls v. American Optical Corp., 740 So.2d 1262, 1271-72 (La.1999). To repeat, the comparative fault statute did not apply to causes of action that accrued after the effective date of the statute; instead, the statute applied to causes of action “arising from events” occurring after the effective date. This unusual statutory language was highly significant in Cole, where the plaintiffs exposure to asbestos (the “events” giving rise to the suit) occurred many years before he suffered damages from the exposure and before his cause of action accrued. The LPLA, on the other hand, applies to causes of action that accrued after the statute’s effective date. For this reason, the “exposure rule” of Cole cannot be read so expansively as to apply to LPLA cases.

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Bluebook (online)
243 F.3d 200, 2001 U.S. App. LEXIS 3466, 2001 WL 170647, Counsel Stack Legal Research, https://law.counselstack.com/opinion/grenier-v-medical-engineering-corp-ca5-2001.