Fleury v. Biomet, Inc.
This text of 865 So. 2d 537 (Fleury v. Biomet, Inc.) is published on Counsel Stack Legal Research, covering District Court of Appeal of Florida primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.
Opinion
Norman C. FLEURY, Jr., and Karen Fleury, Appellants,
v.
BIOMET, INC., a foreign corporation, and Mike Trieste, Appellees.
District Court of Appeal of Florida, Second District.
John P. Graves, Jr., of Graves & Stephan, Chartered, Sarasota, for Appellants.
Marie A. Borland and Robert B. Gough, III of Hill, Ward & Henderson, P.A., Tampa, and A. Lamar Matthews, Jr. of Matthews, Eastmoore, Hardy, Crauwels & Garcia, P.A., Sarasota, for Appellees.
NORTHCUTT, Judge.
Norman Fleury, Jr., and his wife, Karen Fleury, filed a negligence and products liability action stemming from the premature failure of Mr. Fleury's artificial knee. The defendants, Biomet, Inc., and Mike Trieste, won a final summary judgment *538 after the circuit court entered an order imposing sanctions for the spoliation of evidence. We reverse.
For purposes of reviewing the summary judgment, we view the allegations and evidence of record in the light most favorable to the Fleurys, treating any factual disputes as resolved in their favor. Thus viewed, the record reflects the following:
The product at the center of this controversy was an artificial knee that was designed and manufactured by Biomet and sold by Trieste, Biomet's exclusive distributor in Charlotte County, Florida. The specific artificial knee at issue was packaged by Biomet on October 11, 1990, and sterilized the next day. Biomet then placed the knee in its inventory. It remained there until December 1994, when it was employed in a total right knee replacement performed on Mr. Fleury by Dr. Douglas Nuelle, an orthopedic surgeon.
The knee consisted of tibial, patella, and femoral components. This litigation focused on the tibial component, which in significant part was formed by molding a polymer known as ultra-high molecular weight polyethylene, or UHMWPE, to a metal tray. The expected life of a tibial component such as the one implanted in Mr. Fleury is ten to fifteen years. His failed prematurely, after only two years. Eventually, in October 1999, another orthopedic surgeon, Dr. Vance Askins, removed Mr. Fleury's artificial knee and replaced it with another one.
When Dr. Askins performed the 1999 surgery, he found that all three main components of Mr. Fleury's artificial knee-the femoral, patella, and tibial-were loose. The polyethylene that had been molded to the tibial tray had failed. The metal was exposed and there were small pieces of polyethylene floating in Mr. Fleury's knee.
In the litigation the Fleurys and their experts contended that the polyethylene failed because it had oxidized over time due to the process Biomet had employed to sterilize the artificial knee. When the knee was manufactured in 1990, Biomet sterilized it by subjecting it to gamma rays. A Biomet representative testified in deposition that problems with oxidation led the company to alter its sterilization protocol in mid-1992. Henceforth, Biomet sterilized its polyethylene products by subjecting them to gamma rays in an oxygen-free environment, which was achieved by injecting argon gas into the packaging to force out any oxygen. Two years later, when Biomet sold the circa 1990 artificial knee that was implanted in Mr. Fleury, it did not warn that the knee had been sterilized by a method that could cause it to oxidize over time.
The hospital where Dr. Askins performed Mr. Fleury's second knee replacement discarded the Biomet artificial knee within hours after it was removed from Mr. Fleury's leg. This was done pursuant to the hospital's standard protocol for handling and disposing of bio-hazardous waste. Under the protocol, Dr. Askins could have directed the hospital to preserve the knee, but he did not.
About six weeks before the scheduled trial in the Fleurys' lawsuit, Biomet and Trieste moved to dismiss, contending that their inability to examine and test the artificial knee prevented them from defending against the Fleurys' allegations. The defendants filed an affidavit by Stephen Li, Ph.D., the president of a medical device testing company and an expert in polymers used in medical devices. Dr. Li expressed doubt that Mr. Fleury's artificial knee failed because the polyethylene in the tibial component had oxidized. He asserted that there was no clinical or laboratory evidence that a directly molded tibial component *539 that had been gamma sterilized in air would suffer clinically significant oxidation in the first nine years after its irradiation, either on the shelf or implanted. Dr. Li also maintained that it would be impossible to attribute the failure of Mr. Fleury's knee to oxidation without examining and testing the product. He went on to list some of the examinations and tests that might be performed if the product were available.
When ruling on the defendants' motion to dismiss, the circuit court found that none of the parties to the lawsuit were at fault for the loss of the artificial knee, and that the spoliation of this evidence was inadvertent. Still, the court noted that there was some evidence to suggest that before Mr. Fleury's second surgery he and Dr. Askins believed that the Biomet knee was defective. Therefore, although the court declined to dismiss the suit, it ordered that at trial Dr. Askins and the Fleurys' expert witnesses would not be permitted to opine either as to the cause of any observed wear of the artificial knee's polyethylene component or that oxidation contributed to the wear. In addition, the jurors would be instructed that they must presume that the product was not defective.
Thus deprived of their ability to prove the causation element of their cause of action, the Fleurys suffered the summary judgment under review. We reverse because the circuit court should not have entered the spoliation order.
Sanctions for the spoliation of evidence may be imposed when a party fails to preserve evidence in its custody. Under the facts described above, it is debatable whether the subject artificial knee was ever in the Fleurys' custody. See Derosier v. Cooper Tire & Rubber Co., 819 So.2d 143 (Fla. 4th DCA 2002) (holding that spoliation of evidence principles did not apply where tread that had separated from allegedly defective tire had been discarded by persons unknown immediately after automobile accident while plaintiffs were being transported to the hospital, and thus evidence was not in plaintiffs' custody when it was lost), review denied, 837 So.2d 409 (Fla.2003).
Even when it is clear that evidence has been lost while in the custody of a party, the appropriate sanction varies according to the willfulness or bad faith, if any, of the party who lost the evidence, the extent of the prejudice suffered by the other party, and what is required to cure the prejudice. Harrell v. Mayberry, 754 So.2d 742, 745 (Fla. 2d DCA 2000); Sponco Mfg., Inc. v. Alcover, 656 So.2d 629, 630 (Fla. 3d DCA 1995). Dismissal or default, the harshest of all sanctions, are reserved for cases in which one party's loss of evidence renders the opposing party completely unable to proceed with its case or defense. Harrell, 754 So.2d at 745.
In this case, the circuit court determined that neither party was at fault for the loss of the evidence, and that dismissal of the Fleurys' suit would be too harsh a sanction. Yet the court's sanction order accomplished the same result by depriving the Fleurys of any ability to prove a necessary element of their cause of action.
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