Burwell v. American Edwards Laboratories

574 N.E.2d 1094, 62 Ohio App. 3d 73, 1989 Ohio App. LEXIS 823
CourtOhio Court of Appeals
DecidedMarch 9, 1989
DocketNo. 88AP-30.
StatusPublished
Cited by5 cases

This text of 574 N.E.2d 1094 (Burwell v. American Edwards Laboratories) is published on Counsel Stack Legal Research, covering Ohio Court of Appeals primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Burwell v. American Edwards Laboratories, 574 N.E.2d 1094, 62 Ohio App. 3d 73, 1989 Ohio App. LEXIS 823 (Ohio Ct. App. 1989).

Opinion

*76 Young, Judge.

This matter is before this court upon the appeal of James F. Burwell et al., appellants, from a jury verdict rendered in favor of American Edwards Laboratories, Division of American Hospital Supply Corporation et al. (“Edwards”), appellees. Appellant James F. Burwell (“Burwell”) underwent open heart surgery during which his natural heart valve was replaced with an artificial “porcine” valve, the Model 2625 IA (“model 2625” or “IA valve”), which was manufactured by appellees. Approximately five months after his operation, Burwell began to experience such physical difficulties as dizziness, lightheadedness and black-outs. After performing a catherization on Burwell, Burwell’s doctor determined that a problem existed with regard to the flow of blood through Burwell’s heart and that a second open heart surgery would be necessary. Consequently, surgery was performed on Burwell to remove the artificial valve and then replace it with another model 2625 IA valve, also manufactured by appellees.

Appellants thereafter filed a products liability action against appellees based on negligence, breach of express and implied warranties, strict liability, misrepresentation, and loss of consortium for Burwell’s wife and children. The gravamen of appellants’ complaint was that the IA valve which was initially implanted into Burwell’s heart had been defectively manufactured by appellees. Additionally, punitive damages were sought on the grounds that appellees recklessly or intentionally concealed information of the defect.

Prior to trial, appellees filed a multi-branch motion in limine, seeking, inter alia, to exclude evidence relevant to discovery disputes which had occurred between the parties. The motion was granted in part, excluding the evidence.

Jury trial subsequently commenced before a referee, who presided by agreement of the parties. At the close of appellants’ case-in-chief, appellees moved for directed verdict on all claims, which the court granted in part and denied in part. Following presentation of all the evidence, the trial court further directed a verdict in favor of appellees on the issue of punitive damages. Upon deliberation, the jury returned a verdict in favor of appellees. Furthermore, the jury responded unanimously in the negative to a special interrogatory submitted to them which asked: “Did the heart valve implanted in James Burwell in 1981 contain a stainless steel splice?”

Thereafter, the referee filed a report with the trial judge incorporating the jury verdict as well as the verdicts directed against appellants. No objections were filed to the report, which was adopted by the trial court by judgment entry dated April 6, 1987. Appellants subsequently filed a motion for a new *77 trial. The motion was denied, and this appeal ensued with the following eleven assignments of error set forth by appellants:

“I. The trial court committed prejudicial error when it granted defendantappellee’s motion for a directed verdict on the issue of punitive damages after it had previously ruled at the end of plaintiff-appellants’ case that plaintiff-appellants had established a prima facie case which would have supported punitive damages.
“II. The trial court committed prejudicial error when it refused to instruct the jury that defendant-appellee could be held liable under a products liability cause of action if, in fact, the valve implanted in Jim Burwell spontaneously degenerated within five months of implantation as argued by defendantappellees.
“HI. The court erred in instructing the jury, in regard to the cause of action for strict liability and tort, that the strict liability instruction applied even though the seller had exercised all ‘due care’ in the preparation and sale of the product. The law, as developed by the Ohio Supreme Court, states that the strict liability principles apply even though the seller has exercised ‘all possible’ care in the preparation and sale of the product.
“IV. The trial court committed prejudicial error in ruling on plaintiff-appellants’ motion for a new trial prior to the time that referee Roberts, who had sat as the presiding judge on the trial, rendered any report, opinion or other memorandum regarding the motion.
“V. The trial court erred in refusing to allow plaintiff-appellants, in pursuit of their claim that there had been an on-going practice by defendants to cover up known defects in their products, to introduce the evidence it had obtained, that, in a similar case, defendant-appellees has [sic] intentionally misled a court and jury.
“VI. The court erred in refusing to admit plaintiff’s Exhibits 10, 11 and 12 into evidence which showed specifically that Dr. Estes, the president of the corporation, swore that there had never been a recall of the Model 2625 heart valve and did not retract that statement until after all the doctors had been deposed for trial.
“VII. The trial court committed prejudicial error in not admitting into evidence Exhibits 79, 80 and 81 in support of the claim that defendantappellees engaged in a pattern and practice of recklessly disregarding the health and safety of persons receiving their valves.
“VIII. The trial court committed error in granting the motion in limine made by defendant-appellees thereby ordering that the jury was not to be advised of any conduct on the part of defendant-appellee in the discovery *78 process. The trial court further committed prejudicial error in refusing to admit into evidence plaintiffs Exhibits 9, 13 and 13A which document the continuing course of intentional concealment of the defective stainless steel valves from the public in general and from plaintiff-appellants in particular.
“IX. The trial court committed prejudicial error when it refused to instruct jury, pursuant to Ohio Jury Instruction 305.7 on failure to produce evidence.
“X. The verdict rendered by the jury was against the manifest weight of the evidence.
“XI. The trial court committed prejudicial error in refusing to instruct the jury relative to Ohio Jury Instruction 351.02 on failure to warn.”

In their first assignment of error, appellants assert that the trial court erred in directing a verdict in favor of appellees on the issue of punitive damages in light of its prior ruling that appellants had established a prima facie case on that issue. The record demonstrates that, prior to trial and in response to appellees’ motion in limine, the trial court ordered that no evidence of Edwards’ financial net worth be presented to the jury until appellants had established a prima facie case entitling appellants to punitive damages. At the close of appellants’ case, the trial court determined that a prima facie case had been established on the issue of gross negligence or willful and wanton, reckless disregard for the health and safety of others.

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Bluebook (online)
574 N.E.2d 1094, 62 Ohio App. 3d 73, 1989 Ohio App. LEXIS 823, Counsel Stack Legal Research, https://law.counselstack.com/opinion/burwell-v-american-edwards-laboratories-ohioctapp-1989.