Brenda Griffin Toole v. Richmond C. McClintock, Jr

CourtCourt of Appeals for the Eleventh Circuit
DecidedDecember 14, 2000
Docket99-15019
StatusPublished

This text of Brenda Griffin Toole v. Richmond C. McClintock, Jr (Brenda Griffin Toole v. Richmond C. McClintock, Jr) is published on Counsel Stack Legal Research, covering Court of Appeals for the Eleventh Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Brenda Griffin Toole v. Richmond C. McClintock, Jr, (11th Cir. 2000).

Opinion

Brenda Griffin TOOLE, Plaintiff-Appellee-Cross-Appellant, v.

BAXTER HEALTHCARE CORPORATION, Defendant-Appellant-Cross-Appellee.

No. 99-15019. United States Court of Appeals,

Eleventh Circuit. Dec. 14, 2000.

Appeal from the United States District Court for the Northern District of Alabama, (No. 94-13559-CV-P-S), Sam C. Pointer, Jr., Judge.

Before CARNES and BARKETT, Circuit Judges, and POLLAK,* District Judge. BARKETT, Circuit Judge:

Baxter Healthcare Corporation ("Baxter") appeals a final judgment based on a jury verdict in favor of Brenda Toole for injuries she suffered as a result of breast implants manufactured by Heyer-Schulte

Corporation, Baxter's predecessor corporation. In 1987, several years after receiving the implants, Ms. Toole began to experience capsular contracture, a hardening of the breast due to scar tissue around the implant compressing down on the implant.

Her physician performed a "closed capsulotomy"1 to correct the contracture. Ms. Toole's pain continued, leading to surgery which revealed that both implants had ruptured. The implants were replaced.

Approximately one year after the replacement surgery, Ms. Toole discovered a lump in her breast and was forced to undergo the first of multiple surgical procedures to remove what turned out to be silicone granulomas.2 Ms. Toole became increasingly ill, experiencing difficulty concentrating, oral ulcers, hair loss, dry skin, and fatigue. As time passed, she had increasing pain in the form of arthralgias and myalgias. While

disagreeing as to the etiology of the disease, the parties do not dispute that her symptoms were real.

* Honorable Louis H. Pollak, U.S. District Judge for the Eastern District of Pennsylvania, sitting by designation. 1 In performing a closed capsulotomy, the physician attempts to break the scar capsule by manually exerting direct, extreme pressure upon it. At the time, closed capsulotomy was the treatment of choice for contracture. 2 A granuloma is the human body's encapsulation of small amounts of a foreign substance, in this case silicone. Ms. Toole filed this tort action against Baxter.3 Two jury trials were held in this lawsuit. At the first trial, she was awarded $350,000 in compensatory damages and $5,000,000 in punitive damages. Ms. Toole accepted a remittitur of the compensatory damages to $275,000 and punitive damages to $2,000,000, and the

trial court denied Baxter's motions for Judgment as a Matter of Law ("JNOV"). After Baxter appealed, this

Court found that the evidence presented at the first trial was insufficient to support an award of punitive

damages, reversed the compensatory damages based upon an evidentiary issue,4 and remanded the case for

a new trial. Toole v. McClintock, 999 F.2d 1430 (11th Cir.1993) (hereinafter "Toole I ").

In the second trial, the jury awarded $2,500,000 in compensatory damages and $3,500,000 in punitive damages to Ms. Toole. The trial court granted Baxter's Motion for JNOV as to punitive damages and denied

Baxter's Motion for a New Trial on compensatory damages conditioned on Ms. Toole's acceptance of a remittitur of the compensatory damage amount to $1,000,000. Ms. Toole originally rejected the remittitur and the case was restored to the docket for trial. However, prior to trial, Ms. Toole filed, and the trial court

granted, a motion to withdraw her earlier rejection of the remittitur and accept the reduced amount of

$1,000,000 in compensatory damages. Baxter then filed its "renewed" post-trial motions which were denied. Baxter now appeals those denials, and Ms. Toole cross-appeals the punitive damages issue. DISCUSSION

Baxter argues on appeal that the judgment against it must be reversed because the trial court: (1) failed to properly instruct the jury on the duties of a medical device manufacturer; (2) erroneously admitted expert testimony that the implants caused Ms. Toole's injury; (3) erroneously admitted evidence of prior

complaints against the manufacturer about product failures that Baxter asserts were irrelevant and prejudicial; (4) erred in allowing Ms. Toole to accept a remittitur which she had originally rejected; and (5) once having

entered judgment upon Ms. Toole's acceptance of the remittitur, erred in failing to grant Baxter a new trial

under F.R.C.P. 60(b) based on intervening scientific and legal developments relating to breast implants. Ms. Toole cross-appeals, claiming that the trial court erred in vacating the award of punitive damages. We

address each claim in turn.

1. Evidentiary Rulings

3 The original complaint also contained medical malpractice allegations against Ms. Toole's physician, but the jury determined that the doctor was not liable. 4 This evidentiary issue did not arise in the second trial. A. Admission of expert witness testimony

Baxter claims that admitting the testimony of Drs. Schneider, Tiliakos, Gaston and Espinosa, each of whom testified to support Ms. Toole's contention that the breast implants that she received caused her

disease, constituted an abuse of discretion. Baxter likewise claims that the district court erred in admitting

the testimony of Drs. Shanklin, Smalley and Batich, who did not testify to causation directly, but described

a disease process based on the human body's reaction to silica and/or the degradation of silicone into silica, which related to the effects of the residual silicone in Ms. Toole's body from the rupturing of her breast

implants during the closed capsulotomy. Ms. Toole first responds that Baxter did not properly preserve this issue, arguing that objections

which had been made in limine were not renewed at trial and that objections to certain questions posed to the

expert witnesses during trial were insufficient to preserve their Daubert objections. Based on the record, we

are satisfied that Baxter appropriately preserved this issue. Baxter submitted three motions in limine,

objecting to the expert testimony of Drs. Shanklin, Smalley and Batich, respectively. As to the other experts, Baxter lodged objections in the course of the experts' testimony based on a lack of foundation for the opinion. The district court overruled the objections and admitted the testimony. On this record we are satisfied that

the objections were sufficient to preserve the issue. We review a trial court's evidentiary rulings on the admission of expert witness testimony for abuse

of discretion. General Electric Co. v. Joiner, 522 U.S. 136, 142, 118 S.Ct. 512, 139 L.Ed.2d 508 (1997);

see also Kumho Tire Co. v. Carmichael, 526 U.S. 137, 142, 119 S.Ct. 1167, 143 L.Ed.2d 238 (1999).

Scientific evidence or testimony must not only be relevant, but also reliable. Daubert v. Merrell Dow

Pharmaceuticals, Inc., 509 U.S. 579, 589, 113 S.Ct. 2786, 125 L.Ed.2d 469 (1993). Accordingly, we grant

the district court the same broad latitude when deciding how to determine the reliability of expert testimony

as it enjoys in determining whether the testimony is reliable. Kumho Tire Co., 526 U.S. at 142, 119 S.Ct.

1167.

Under Federal Rule of Evidence 702 and Daubert, expert testimony is admissible if (1) the expert

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