Marks v. Minnesota Mining & Manufacturing Co.

187 Cal. App. 3d 1429, 232 Cal. Rptr. 594, 1986 Cal. App. LEXIS 2352
CourtCalifornia Court of Appeal
DecidedNovember 20, 1986
DocketA026069
StatusPublished
Cited by21 cases

This text of 187 Cal. App. 3d 1429 (Marks v. Minnesota Mining & Manufacturing Co.) is published on Counsel Stack Legal Research, covering California Court of Appeal primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Marks v. Minnesota Mining & Manufacturing Co., 187 Cal. App. 3d 1429, 232 Cal. Rptr. 594, 1986 Cal. App. LEXIS 2352 (Cal. Ct. App. 1986).

Opinion

Opinion

NEWSOM, J.

The present appeal is from judgment following a jury verdict in plaintiff’s favor in a products liability action. The product involved *1431 is an inflatable mammary prosthesis used in breast augmentation surgery. Following the verdict, the trial court granted a motion notwithstanding the verdict and deleted the jury’s award of $75,000 in punitive damages. Plaintiff appeals, seeking reversal of the judgment regarding punitive damages. Defendants cross-appeal, urging that the award of compensatory damages be reversed.

A brief summary of the procedural background reveals the following. On January 20, 1982, plaintiff filed a complaint for strict products liability, breach of warranty, and negligence against Minnesota Mining and Manufacturing Company (3M) and McGhan Medical Corporation. 3M and McGhan Medical Corporation promptly filed separate answers to the complaint. On November 3, 1982, after a noticed motion, plaintiff filed a first amended complaint which added a claim for punitive damages and specifically named McGhan Medical Corporation, a California Corporation (McGhan/Cal.), McGhan Medical Corporation, a Delaware Corporation (McGhan/Del.), and McGhan Medical/3M, a division of 3M (McGhan/3M) as defendants.

The case was submitted to the jury solely on a theory of strict products liability. Following a 10-day trial, the jury returned a verdict in favor of plaintiff, assessing compensatory damages of $25,850 and punitive damages of $75,000 against 3M and McGhan/3M. After entry of judgment on the verdict, defendants moved for a new trial and for judgment notwithstanding the verdict. The motion for new trial was denied, but a judgment notwithstanding the verdict was entered deleting the award of punitive damages. Plaintiff filed a timely notice of appeal on February 6, 1984, and defendants cross-appealed.

In relevant part the factual background may be summarized as follows. In November 1974, five former employees of Heyer-Schulte Corporation, a medical products manufacturer, formed McGhan Medical Corporation, a California corporation. In the fall of 1975, the founders of McGhan/Cal. decided to manufacture an inflatable mammary prosthesis, or implant, for use in breast augmentation surgery. 1 Production of the McGhan inflatable prosthesis began in October 1975 and the product was generally available for sale to physicians by early 1976.

In early 1977 plaintiff decided to have breast augmentation surgery. Dr. Robert Kropp performed the surgery in April 1977, using two McGhan *1432 inflatable implants. In June of the same year, McGhan/Cal. was acquired by a wholly owned Delaware subsidiary of 3M which was also named McGhan Medical Corporation. 2 McGhan/Del. continued to manufacture and market the McGhan inflatable implant without alteration.

In May 1978 an internal company memorandum reported on complaints about the inflatable and noted its “alarming rate” of deflation. From 63 complaints in 1976, and an equal number in 1977, the number rose to 160 in 1978. In June 1978 an agent from the Federal Food and Drug Administration, which oversees the manufacture of such medical devices, came to McGhan/Del. for an inspection. 3 The inspector requested but was refused access to complaint files by Laurens Wallace, a McGhan/Del. quality assurance supervisor.

In October 1978 plaintiff’s left implant spontaneously deflated. Neither plaintiff nor her doctor knew the cause. Plaintiff thereupon underwent a second surgery in which the deflated implant was replaced with another McGhan product. Unlike the first two implants, the new left implant had been manufactured by McGhan/Del., after the 3M acquisition.

In April 1979 the McGhan inflatable prosthesis was removed from the market. One of the reasons for removing the product was the troublesome rate of deflations being reported to the company. A cause of these deflations was the tendency of the thin shell of the implant to crease inside a woman’s body. Leaks in the shell would then develop along the crease. Formation of the creases was aggravated by normal contractions of tissue around the implant.

In May 1979 plaintiff’s right implant spontaneously deflated. In a third surgery, the implant was replaced with a Heyer-Schulte implant. By this time, plaintiff’s doctor had noted a number of deflations of McGhan implants and had discontinued use of the McGhan product.

*1433 In August 1979, complaints regarding the McGhan inflatable resulted in a second inspection by the FDA. At this time, Wallace—rather than allowing access to the complaint files—provided the inspector with graphs portraying the number of deflations of inflatables. The graphs indicated that as of April 1979, 158 complaints had been received. 4 In April 1980 the FDA again requested the number of complaints received regarding inflatables and was told that there were 500 to 600 complaints.

On January 1, 1981, 3M’s wholly owned subsidiary (McGhan/Del.) was reorganized as a division of 3M and dissolved. From that date forward, the McGhan operations were conducted by 3M.

In November 1981 plaintiff’s left implant (the third McGhan inflatable) deflated and was replaced in a fourth surgery with a Heyer-Schulte implant. In January 1982 the complaint was filed. 5

On appeal, plaintiff argues that the order granting 3M’s motion for judgment notwithstanding the verdict as to punitive damages was incorrect on both the legal and factual bases enumerated in the order. The precise statement of the trial court in support of its order deleting the jury’s award of punitive damages was as follows: “Said Order is based on the determination of the Court that:

“ 1. Defendant corporations as successor corporations to the manufacturer of the product were not liable for punitive damages, and
“2. There was no evidence of sufficient substantiality to establish malice, that is, conduct which was intended to cause injury to the Plaintiff or conduct carried on by the Defendants with a conscious disregard of the rights and safety of the Plaintiff.” *

Before plunging into the intricacies of the McGhan-3M relationship, we note that 3M neither designed nor manufactured the implant that injured plaintiff. McGhan/Cal. and its original founders conceived the design and first manufactured and marketed it. According to plaintiff’s expert, McGhan/ *1434 Cal. knew of the design problems, did not properly test the product, and received the initial complaints. McGhan/Del., the 3M subsidiary, actually manufactured and sold the third implant that injured plaintiff. It received many additional complaints and inquiries from the FDA, but continued to market the product without change. Eventually, and prior to its merger with 3M, McGhan/Del. removed the product from the market.

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Cite This Page — Counsel Stack

Bluebook (online)
187 Cal. App. 3d 1429, 232 Cal. Rptr. 594, 1986 Cal. App. LEXIS 2352, Counsel Stack Legal Research, https://law.counselstack.com/opinion/marks-v-minnesota-mining-manufacturing-co-calctapp-1986.