Pfizer, Inc. v. Stryker Corp.

385 F. Supp. 2d 380, 2005 WL 2155224
CourtDistrict Court, S.D. New York
DecidedAugust 7, 2005
Docket02 Civ. 8613(LAK)
StatusPublished
Cited by3 cases

This text of 385 F. Supp. 2d 380 (Pfizer, Inc. v. Stryker Corp.) is published on Counsel Stack Legal Research, covering District Court, S.D. New York primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Pfizer, Inc. v. Stryker Corp., 385 F. Supp. 2d 380, 2005 WL 2155224 (S.D.N.Y. 2005).

Opinion

MEMORANDUM OPINION

KAPLAN, District Judge.

This is an action principally for alleged breach of defendants’ obligation to indemnify plaintiffs for losses incurred as a result of products liability claims arising from the sale of knee implants following the transfer by plaintiffs to defendants of plaintiffs’ knee implant business. The Court previously granted summary judgment for plaintiffs as to liability on the principal claims. Plaintiffs’ damage case was tried to a jury, which returned a verdict aggregating more than $13 million. The matter now is before the Court on defendants’ post-verdict motion for judgment as a matter of law dismissing certain of plaintiffs’ damage claims.

Background,

A The Dispute

The broad contours of this dispute have been outlined in a number of opinions and orders, 1 and only a few facts need be repeated here.

In 1998, Pfizer 2 sold its prosthetic joint and implant business to Stryker for $1.6 billion. The Stock and Asset Purchase Agreement (“Purchase Agreement”) provided, in pertinent part, that Pfizer would retain responsibility for third party product liability claims arising in respect of prosthetic joints sold on or prior to the closing, while Stryker would be responsible for claims relating to joints sold after the closing. After the deal closed, the parties were sued on a number of claims arising from the sale of the Duracon Uni-compartmental Knee (“DUK”), one of the products of the acquired business.

Pfizer brought this action against Stryker for a declaratory judgment and breach of contract for failing to indemnify it for expenses incurred from third party product liability suits brought in respect of DUKs sold after the closing. Stryker countersued principally for misrepresentation, breach of warranty and fraud. This Court granted Pfizer’s motion for summary judgment to the extent of declaring that it is entitled to indemnification by Stryker for all Losses, other than punitive damages, incurred in respect of DUKs sold after the closing. 3 Stryker’s cross-motion for summary judgment was denied in all respects. Pfizer’s damage claim was tried to a jury on March 22, 23 and 24, 2005.

*383 B. The Damages Trial

By the time the case was submitted to the jury, there were three issues, 4 only two of which are disputed here. 5

1. Orrik Claims

The first concerned the so-called Orrik litigation, which involved forty plaintiffs, twenty-nine of whom received DUKs sold after the closing. On the second day of the Orrik trial, Pfizer and Stryker settled with all forty plaintiffs for a lump sum of $13.25 million. Stryker contributed $3.25 million, which the parties agreed would go only to the post-closing claimants, toward the global settlement. Pfizer contributed the remaining $10 million. It here claimed that $6,275 million of that amount went to post-closing plaintiffs and therefore is recoverable from Stryker under the Purchase Agreement.

Pfizer’s evidence concerning this issue at the damages trial consisted principally of the testimony of its counsel in the Orrik case and the individual releases executed by the Orrik plaintiffs, which showed the amount that each received as consideration for dismissing his or her claim. 6 This evidence showed that the post-closing claimants had received $9,525,000 from the global settlement, $3.25 million of which had been contributed by Stryker.

Stryker offered testimony that it had approved only a lump sum settlement of $13.25 million to the plaintiffs and had not agreed to whatever allocation the Orrik plaintiffs made among themselves. 7 It offered an e-mail that purported to reserve Stryker’s rights to resolve the allocation among the twenty-nine post-closing plaintiffs. 8 It offered also various letters between the Pfizer and Stryker trial teams discussing the Orrik settlement that similarly reserved each party’s rights under the Purchase Agreement. 9

2. Legal Expenses

The second issue that remains pertinent here concerns the legal expenses incurred by Pfizer for which it seeks indemnification.

The evidence at trial was to the effect that Pfizer’s products liability counsel created files denominated “DUK General,” “Orrik General” and “Bartlett General” that Pfizer claimed were used to record expenses incurred for services applicable to the defense of cases involving implants sold both before and after the closing. The DUK General file, for example, was a billing code for activities that were useful in every case involving a DUK, such as interviewing an engineer involved in its design, 10 irrespective of whether the DUK *384 was sold before or after the closing of the sale of the business. In addition, Pfizer adduced evidence that its product liability counsel had done more work to handle the general background matters and had utilized more of the firm’s associates to help with the litigation once it became clear that Stryker would not defend the post-closing cases. 11

Pfizer claimed that Stryker was obliged to indemnify it for a proportion of the “general” expenses equal to the proportion of post-closing cases to the total number of cases. It offered a summary exhibit that listed the total billings and the pro rata share attributable, on its theory, to post-closing cases. With respect to the Orrik litigation, for example, the summary exhibit listed the legal billings to the Orrik general file by the firm of Goodell Devries Leech & Dann, LLP as totaling $176,065.30 and attributed 29/40th of that amount-$127,647.34-to the post-closing cases. 12

3. The Verdict

At the close of the evidence, Stryker moved for judgment as a matter of law pursuant to Federal Rule of Civil Procedure 50(a). It was denied and the case went to the jury. On March 24, 2005, the jury returned with a verdict for Pfizer. The jury found that Pfizer paid $6,275,000 to settle post-closing cases in the Orrik litigation and that no part of that amount was paid in respect of claims for punitive damages. It further found that $1,153,034.97 of the legal expenses billed to the general files — which represented half of the total billings to the general files— was attributable to post-closing cases. 13

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Cite This Page — Counsel Stack

Bluebook (online)
385 F. Supp. 2d 380, 2005 WL 2155224, Counsel Stack Legal Research, https://law.counselstack.com/opinion/pfizer-inc-v-stryker-corp-nysd-2005.