Cerabio LLC and Phillips Plastics Corporation v. Wright Medical Technology, Inc.

410 F.3d 981, 2005 U.S. App. LEXIS 11066, 2005 WL 1385289
CourtCourt of Appeals for the Seventh Circuit
DecidedJune 13, 2005
Docket04-1171
StatusPublished
Cited by61 cases

This text of 410 F.3d 981 (Cerabio LLC and Phillips Plastics Corporation v. Wright Medical Technology, Inc.) is published on Counsel Stack Legal Research, covering Court of Appeals for the Seventh Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Cerabio LLC and Phillips Plastics Corporation v. Wright Medical Technology, Inc., 410 F.3d 981, 2005 U.S. App. LEXIS 11066, 2005 WL 1385289 (7th Cir. 2005).

Opinion

ROVNER, Circuit Judge.

In this contract dispute, CERAbio, LLC and its sole member, Phillips Plastics Cor *984 poration (collectively “CERAbio”), claims that it delivered all of the assets of the corporation, including its technological know-how, to Wright Medical Technology, Inc. (Wright), but that Wright failed to pay the remaining half of the agreed-upon sales price. Wright countered that not only was the technological knowledge provided by CERAbio worthless and that it therefore had not performed its end of the deal, but that CERAbio had also committed fraud and had been negligent both in the formation and performance of the contract. Upon CERAbio’s motion, the district court granted summary judgment on Wright’s tort counter claims. At trial, the jury ruled in favor of CERAbio on the contract claims. On appeal, Wright challenges the district court’s ruling on summary judgment as well as an evidentiary ruling at trial. We affirm the summary judgment ruling, but reverse and remand to the district court to correct the effect of the erroneous evidentiary ruling, which we agree was in error.

I.

Wright designs, manufactures, and sells medical devices and products, including bone replacement products known as biologies, frequently used during implantation surgery to replace lost bone and provide a framework for new bone growth. In the late 1990’s, CERAbio developed a bone replacement product made from tricalcium phosphate (“TCP”). The Food and Drug Administration approved the new product, Apatight, for use in humans as a bone void filler. CERAbio obtained patents for the Apatight production process and material.

In early 2001, Wright representatives learned about Apatight at a trade conference. CERAbio was strictly a research and development company which did not manufacture or sell Apatight or other products commercially. Wright markets and sells biologies worldwide and was looking to expand its product offerings in the bone replacement market, so a match seemed ideal. CERAbio negotiated with Wright to provide Apatight to Wright which Wright would then market and sell. Eventually, the negotiations evolved and Wright decided to purchase substantially all of CERAbio’s assets, including all patents and know-how.

Prior to entering into the Agreement, CERAbio informed Wright that it had an established and repeatable process for producing Apatight and that all of the raw materials necessary were commercially available. Under the terms of the August 5, 2002 Agreement between the parties (“Agreement”), Wright agreed to pay $3 million for the CERAbio assets with $1.5 million payable upon closing and a second installment of $1.5 million due no later than three days after Wright verified that it was able to produce Apatight (“Verification”). The contract defined the parameters of Verification and required that CERAbio transfer assets to Wright, that it train Wright’s employees, and that Wright produce three test lots of Apatight using the specific work instructions supplied by CERAbio. Wright had sixty days to attempt to produce the three test lots of Apatight in its Memphis facility using commercially reasonable efforts. If it failed to do so, under the Agreement, CERAbio would have the opportunity to access Wright’s manufacturing equipment and cooperate with Wright to produce the three Apatight test lots — again, using commercially reasonable efforts.

After the closing, Wright attempted to buy TCP powder, one of the key raw materials needed to manufacture Apatight, but found that it was no longer available. Plasma Biotal, the manufacturer of the necessary TCP powder, had started making a new TCP powder with a different particle size — one that would not work properly utilizing the Apatight manufac *985 taring instructions. Plasma Biotal still had a limited supply of the original powder, but it had become contaminated. Wright and CERAbio dispute when CERAbio became aware that the powder was unavailable and the role that the unavailability of the powder played in the ability to seal the deal. From this point forward, the statements of facts in the two briefs begin to read like two unrelated novels. When the facts are digested, however, it appears that the parties do not wholly dispute the course of events, but instead dispute where the blame lies.

According to the appellant Wright, CERAbio knew prior to closing on the Agreement that the TCP powder was unavailable, but nevertheless represented to Wright that all of the materials necessary to produce Apatight were generally commercially available. To support this claim, Wright points to the deposition of CERAbio’s senior product development engineer, Dr. Ying Ko, who testified that CERAbio knew prior to closing that the TCP powder was no longer available. CERAbio does not necessarily disagree that it knew of the availability problem, it focuses instead on the fact that it was possible to work around the problem and to produce Apatight without the original TCP powder. And so while it may have known that one form of the powder was unavailable, CERAbio says, it thought that other powders were available and acceptable alternatives. It thus counters Dr. Ko’s testimony by pointing to evidence that Plasma Biotal had assured Dr. Ko that it could produce an “original style” powder. Supp.App. at 4. 1 It further implies also that even if CERAbio did know that the powder was unavailable, the Agreement between the two parties put the onus on Wright to engage in due diligence in order to verify the availability of all necessary materials. Finally, it claims that Wright itself was aware of the powder unavailability problem prior to the closing. CERAbio’s spin, in’ a nutshell, is that the unavailability of the TCP powder was not CERAbio’s fault and that with some revisions to the work instructions Apatight could be produced using the new powder, but that Wright never gave CERAbio the chance. It also argues that Wright eventually found a manufacturer who could make a “lookalike” powder but decided instead to shut CERAbio out of the process, produce the virtually identical ceramic bone replacement, Cellplex, on its own, and claim it as its own new creation to avoid paying the remainder of the $1.5 million fee and royalties. 2

Wright, of course, has a different story to tell. Shortly after closing, CERAbio informed Wright that the instructions had to be changed due to the unavailability of the TCP powder- — -a problem that CERA-' bio claimed not to have known about prior to closing on the Agreement. Wright claims that, based on these representations, it consented to oral modifications of the Agreement — permitting CERAbio to make changes to the work instructions and to attempt twelve “pre-verification” production funs over the course of several months. Wright points to evidence that CERAbio did, in fact, know about the availability problem prior to closing and argues that had it known that CERAbio had hidden its knowledge of the unavaila *986 bility, it never would have agreed to the modification.

In the meantime, in light of the powder unavailability, efforts to resolve the problem proceeded on two fronts.

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Bluebook (online)
410 F.3d 981, 2005 U.S. App. LEXIS 11066, 2005 WL 1385289, Counsel Stack Legal Research, https://law.counselstack.com/opinion/cerabio-llc-and-phillips-plastics-corporation-v-wright-medical-technology-ca7-2005.