In Re Diet Drugs (Phentermine/Fenfluramine/Dexfenfluramine) Products Liability Litigation

93 F. App'x 345
Court of Appeals for the Third Circuit·Decided February 23, 2004·No. 02-3529·Unpublished·Cited by 4 cases

Opinion

OPINION

CHERTOFF, Circuit Judge.

This appeal is taken from the District Court’s Pretrial Order No. (PTO) 2567 by class members who exercised an intermediate opt-out of the nationwide Diet Drug settlement agreement. Their subsequent state lawsuits were removed to the MDL court from the Louisiana state courts and appellants sought to have their tort cases remanded to state courts, arguing that certain defendants did not consent to removal. PTO 2567 declined to remand appellants’ actions on the grounds that the non-consenting defendants had been collusively joined. Appellants seek review of the District Court’s determination, and an order remanding the cases to the Louisiana state courts. We conclude that we lack jurisdiction to entertain the appeal.

I.

We have previously set forth the basic facts in the Diet Drug litigation. See In re Diet Drugs, 282 F.3d 220 (3d Cir.2002). Because this opinion is written only for the parties, we recite only the facts relevant to our decision.

Prior to 1997, Wyeth, then named American Home Products, 1 sold two prescription drugs for the treatment of obesity, Pondimin and Redux. In September 1997, the United States Food and Drug Administration (FDA) issued a press release stating that a “higher than expected percentage of’ patients taking the drugs “had abnormal echocardiograms, even though they had no symptoms.” Press Release, FDA, FDA Announces Withdrawal Fenfluramine and Dexfenfluramine (Fen-Phen) (Sept. 30, 1998). In response to that press release, Wyeth voluntarily withdrew the products from the market. Prior to Wyeth having done so, however, some 5.8 million individuals had used one or the other of the two drugs. Subsequent stud *347 ies suggest that the drugs may be linked to serious cardiopulmonary side effects-primarily, heart valve regurgitation (the reverse flow of blood through a closed valve of the heart). It is those side effects that are the subject of the Diet Drug litigation at hand.

The federal Diet Drug actions were consolidated for pretrial purposes in the Eastern District of Pennsylvania pursuant to MDL 1203 and, in 1999, Wyeth entered into a Nationwide Class Action Settlement Agreement (the “Settlement Agreement”), executed and approved in that court. The Settlement Agreement set up a multi-tiered framework for benefit entitlement and the filing, processing, and payment of claims. The Settlement Agreement permits class members who satisfy a series of requirements to opt-out of the settlement and back into the tort system at an intermediate point, subject to certain restrictions.

Appellants are forty-eight intermediate opt-outs from the Settlement Agreement. On June 5, 2001, appellants, along with two other intermediate opt-outs, Crystal Gatlin and Yerna Brown (collectively with appellants, the “intervenors”), filed their tort action in Louisiana state court by intervening in an already existing state Diet Drug case. The intervention petition named Wyeth as a defendant, along with eight manufacturers of phentermine (the “phentermine defendants”) whose citizenship was diverse from all of the intervenors, and three Louisiana physicians, whose citizenship was not diverse from any of the intervenors. It was undisputed before the District Court that only Gatlin and Brown had actually been treated by any of the Louisiana defendants.

On July 12, 2001, Wyeth moved to remove the case to federal court. That motion was granted, and the case was ultimately transferred to the Eastern District of Pennsylvania pursuant to MDL 1203. The intervenors, appellants included, requested that the MDL court remand the case to the Louisiana courts, arguing that Wyeth had not shown that all defendants-specifically the phentermine defendants— had consented to removal. Wyeth, for its part, argued that the non-consent of the phentermine defendants was collusive, and that the intervenors lacked an intent to pursue judgment against either the phentermine defendants or the non-diverse physician defendants. The intervenors disputed Wyeth’s contentions.

Limited discovery ensued and, on July 16, 2002, the District Court held a hearing to determine whether remand was appropriate. On August 28, 2002, the District Court issued PTO 2567 denying appellants’ request for remand, but granting the remand requests of intervenors Gatlin and Brown-the only two intervenors who had been treated by the Louisiana physician defendants. 2 Appellants timely appealed. On September 24, 2002, this Court requested letter briefing with respect to a possible jurisdictional defect.

II.

Appellants urge this Court to consider the appeal on two grounds. Apparently conceding that PTO 2567 is not a final order under 28 U.S.C. § 1291, 3 appel *348 lants first urge this Court to reach the merits of their appeal pursuant to the collateral order doctrine as announced in Cohen v. Beneficial Indus. Loan Corp., 337 U.S. 541, 545, 69 S.Ct. 1221, 93 L.Ed. 1528 (1949), and its progeny. As a fallback, appellants urge this Court to exercise its authority to issue a writ of mandamus under the All Writs Act. See 28 U.S.C. § 1651. Finding neither basis for jurisdiction to apply, we will dismiss the appeal.

A.

The collateral order doctrine holds that a non-final order may yet be grounds for appeal if the order: “[(1)] conclusively determinéis] the disputed question, [(2)] resolve[s] an important issue completely separate from the merits of the action, and [(3) is] effectively unreviewable on appeal from a final judgment.” Carr v. Am. Red Cross, 17 F.3d 671, 675 (3d Cir.1994) (internal quotations omitted); see also Cohen, 337 U.S. at 545. All three prongs must be satisfied before an appellate court will review an otherwise interlocutory order. Carr, 17 F.3d at 675. No one contests that PTO 2567 “conclusively determine[d]” the question of remand, and that resolution of the question of remand was “completely separate from the merits of the action .... ” Id. The only question, therefore, is whether PTO 2567 is “effectively unreviewable on appeal from a final judgment.” Id.

Appellants raise three arguments in favor of a finding that PTO 2567 would be essentially unreviewable if we rule that interlocutory review is unavailable. First, appellants argue that they would be relegated to the “slow-moving MDL pretrial process,” and be kept from a more rapid judgment that, they assert, would be available in state courts. Appellant’s Letter Br. at 11. Second, appellants argue that interlocutory review is required because PTO 2567 fails to honor Settlement Agreement terms that, they argue, implicitly “include[d] a strong presumption honoring [opt-outs’] choice of forum.” Appellant’s Letter Br. at 11.

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In Re Diet Drugs (Phentermine/Fenfluramine/Dexfenfluramine) Products Liability Litigation, 93 F. App'x 345 (3d Cir. 2004).

93 F. App'x 345 (In Re Diet Drugs (Phentermine/Fenfluramine/Dexfenfluramine) Products Liability Litigation) — published by Counsel Stack Legal Research, free access to 12M+ legal documents.

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