LeRay v. St. Paul Fire and Marine

444 So. 2d 1252
CourtLouisiana Court of Appeal
DecidedApril 13, 1984
Docket82-CA-0843
StatusPublished
Cited by9 cases

This text of 444 So. 2d 1252 (LeRay v. St. Paul Fire and Marine) is published on Counsel Stack Legal Research, covering Louisiana Court of Appeal primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
LeRay v. St. Paul Fire and Marine, 444 So. 2d 1252 (La. Ct. App. 1984).

Opinion

444 So.2d 1252 (1983)

Randall Albert LeRAY
v.
ST. PAUL FIRE AND MARINE INSURANCE COMPANY, et al.

No. 82-CA-0843.

Court of Appeal of Louisiana, First Circuit.

November 22, 1983.
Opinion Concurring in Part, Dissenting in Part November 30, 1983.
Concurring Opinion December 1, 1983.
Rehearing Denied February 14, 1984.
Writ Granted April 13, 1984.

*1253 Paul H. Due and Charles F. Duchein, III, Baton Rouge, for plaintiff-appellee.

Donald T.W. Phelps, Baton Rouge, and Lloyd W. Hayes, New Orleans, for defendants-appellees *1254 St. Paul Fire and Marine Ins. Co., Dr. B. Eugene Berry, Drs. Acree, Davis and Berry (A Professional Medical Corp.).

Roger M. Fritchie, H. Evans Scobee, Baton Rouge, Robert E. Leake, Jr., New Orleans, for defendant-appellant American Hosp. Supply Corp. (Edwards Laboratories Div.).

Before EDWARDS, WATKINS and SHORTESS, JJ.

EDWARDS, Judge.

Plaintiff obtained a $3,640,000.00 damage judgment against defendant American Hospital Supply Corporation, Edwards Laboratories Division. Edwards Labs appeals. We affirm.

BACKGROUND FACTS

On August 20, 1976, plaintiff was admitted to the Baton Rouge General Hospital, suffering from multiple pulmonary emboli. This is a condition when blood clots (emboli) migrate from the lower extremities and lodge in the lungs, causing decreased respiration, lung damage, and in some instances, death.

On the following day, Dr. B. Eugene Berry, a thoracic and cardiovascular surgeon, was consulted by the admitting physician. Dr. Berry recommended the insertion of a 28 mm Mobin-Uddin umbrella filter in plaintiff's inferior vena cava. This filtering device, manufactured by Edwards Labs, would block the migration of blood clots to plaintiff's lungs.

The 28 mm filter was implanted without complication on August 21, 1976. However, several days later, it was discovered that the filter had unseated from the vena cava and migrated to the right lung, lodging in plaintiff's right pulmonary artery. Dr. Berry allowed plaintiff's condition to stabilize for a few hours and then proceeded to surgically remove the filter. However, during this operation, plaintiff suffered an extended period of hypotension or low blood pressure, causing oxygen deprivation of the brain. As a result, plaintiff incurred permanent brain damage.

Suit was subsequently brought against Dr. Berry and his insurer, St. Paul, and Edwards Labs Division of American Hospital Supply Corporation. Plaintiff alleged negligence on the part of Dr. Berry and defective design (strict liability) by Edwards Labs. A few days before trial, plaintiff settled with Dr. Berry and St. Paul for $750,000.00. After trial, the jury returned a verdict holding Edwards Labs liable to plaintiff and finding no negligence by Dr. Berry.

In this appeal, Edwards Labs, defendant, alleges numerous errors, which we will now consider.

MOTION FOR DIRECTED VERDICT

As plaintiff's suit against defendant was grounded in strict design products liability, his burden was to establish a defect in defendant's filter which caused his injuries. Defendant, however, alleges that plaintiff failed to meet this burden and, therefore, its motion for a directed verdict should have been granted. The trial judge denied the motion, stating that he felt "that there is sufficient evidence upon which reasonable minds could differ and that being the test, [the] motion is overruled." Our review of the record demonstrates that the judge's ruling was correct.

JURY INSTRUCTIONS

At the close of the trial, the jury was instructed by the judge on the standard of liability to be applied to defendant. As for the instruction regarding the definition of a "defect", the judge stated to the jury that:

"A product is defective or unreasonably dangerous when a reasonable seller would not sell the product if he knew the risk involved or if the risks are greater than a reasonable buyer would expect." (Trial p. 1367)

The jury was then instructed to assess defendant's liability under this standard. Defendant contends that this definition is improper and resulted in an erroneous verdict.

*1255 Defendant submits that the determination of a design defect involves the consideration of the product's benefits, risks, and purpose. Hunt v. City Stores, 387 So.2d 585 (La.1980). Defendant asserts that such a "balancing test" instruction to the jury would have resulted in a verdict of dismissal.

However, our examination of the jurisprudence indicates that the judge's definition of "defect" is accurate. The Supreme Court in DeBattista v. Argonaut-Southwest Ins. Co., 403 So.2d 26 (La.1981) and Hebert v. Brazzel, 403 So.2d 1242 (La. 1981), defines a defective or unreasonably dangerous product as one that is dangerous to an extent beyond that which would be contemplated by an ordinary consumer. This shift to a consumer expectation approach for determining defectiveness impliedly rejects the prior balancing test of Hunt, supra, and supports the instruction given the jury.

VERDICT UNSUPPORTED BY EVIDENCE

David Chonette, president of Edwards Labs, testified that they were aware of the migration problems of the 28 mm filter by 1974. Attempts were then made to incorporate hooks on the filter to improve seating and eliminate migration, but these were abandoned. Chonette further stated that the hooks would probably not prevent migration anyway, as he felt the filter's inability to expand past 28 mm was the true cause of the migration problem.

The hook idea came from a competitor's filtering device, known as the Kimray-Greenfield (KG) filter, which has small recurved hooks for engaging the walls of the vena cava. Additionally, the design of the KG filter permits it to expand with the vena cava up to approximately 40 mm. Unlike defendant's filter, the KG filter had no reported instances of migrating to the upper body.

Although fully aware of the risks (i.e., lung damage, impaired respiration, death) that migration posed, defendant continued to market and sell its filter. These risks, of which plaintiff was not informed, are certainly greater than a reasonable consumer would expect, especially in the present situation where defendant should have made further attempts to improve or redesign its product in light of its known deficiencies and the existing technology.

The record contains sufficient evidence to furnish a reasonable basis for the determination that defendant's filter was defective, and therefore, the jury verdict of liability is not manifestly erroneous. Arceneaux v. Domingue, 365 So.2d 1330 (La. 1978).

NEGLIGENCE OF DR. BERRY

Defendant asserts that the jury erred in finding Dr. Berry not negligent in his treatment of plaintiff. Specifically, defendant points to testimony alleging that Dr. Berry implanted the filter at an improper angle; that heparin therapy or ligation of the vena cava was preferable to filter implantation; that plaintiff's consent to the filter insertion was made without adequate disclosure of the risks involved; and that the subsequent operation to remove the filter was negligently performed by Dr. Berry.

However, the record also contains equally strong testimony refuting all of the above alleged facts. Rather than delineate the testimony of the six expert witnesses (five medical doctors and one biomedical engineer), it suffices to say that there is sufficient evidence in the record to supply a reasonable factual basis for the jury verdict absolving Dr. Berry of negligence.

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Bluebook (online)
444 So. 2d 1252, Counsel Stack Legal Research, https://law.counselstack.com/opinion/leray-v-st-paul-fire-and-marine-lactapp-1984.