Rivera v. Wyeth-Ayerst Laboratories

283 F.3d 315, 2002 WL 230657
Court of Appeals for the Fifth Circuit·Decided February 22, 2002·No. 01-40122·Published·Cited by 36 cases

Opinion

JERRY E. SMITH, Circuit Judge:

Pursuant to Fed.R.Civ.P. 23(f), defendants Wyeth-Ayerst Laboratories (“Wyeth”) and American Home Products Corporation appeal the certification of a nationwide class of drug purchasers and their insurance companies. Because we conclude that this suit does not present a justiciable case or controversy under Article III of the Constitution, we reverse and render a judgment of dismissal.

I.

In July 1997, Wyeth began distributing Duract, a non-steroidal anti-inflammatory drug (“NSAID”) prescribed for short-term management of acute pain. Although all NSAID’s carry certain risks of liver and gastrointestinal damage, clinical trials revealed that Duract had additional negative effects. Wyeth included a package insert in each box of Duract detailing these dangers, reporting the results of the clinical trials, recommending Duract be used for only short periods (“generally less than ten days”), and warning that Duract may not be appropriate for those with preexisting *317 liver conditions. The Food and Drug Administration (“FDA”) approved Duraet, its labeling, and its package insert.

In December 1997, Wyeth received three reports of liver failure by patients who had taken Duraet for long-term relief without undergoing liver testing. In February 1998, after receiving FDA approval, Wyeth issued a new, revised package insert reporting these cases of liver failure and reemphasizing that Duraet was intended “only for the short term (10 days or less).” After receiving new reports of liver failure among long term users, Wyeth voluntarily withdrew Duraet from the market in June 1998.

Wyeth explained that of the twelve patients injured by Duraet, eleven had taken the drug for over ten days, and one had preexisting liver disease. Wyeth stated that because no change in Duract’s package insert could guarantee physicians would stop prescribing the drug for long-term use, it was withdrawing Duraet from the market. Wyeth established a program to refund Duraet users for any unused portion of their prescription.

II.

Elizabeth Rivera and the Arkansas Carpenters Health and Welfare Fund (the “Fund”) filed this nationwide class action suit. Rivera seeks to represent all patients who were prescribed, had purchased, and had ingested Duraet but suffered no physical or emotional 1 injury. In fact, the class explicitly excludes any patients who have been injured by Duraet. Nor do plaintiffs claim Duraet was ineffective as a pain killer or has any future health consequences.

Although the class includes citizens of all fifty states and the District of Columbia, plaintiffs state their complaint under Texas law. They allege that Wyeth failed to warn of Duract’s dangers and that Duraet was defective in violation of (1) the Texas Deceptive Trade Practices Act (“DTPA”), Tex. Bus. & Com.Code §§ 17.50, 17.46 (Vernon Supp.1998), (2) the implied warranty of merchantability, Tex. Bus. & Com.Code § 2.314(a) (Vernon 1994), and (3) common law unjust enrichment, and thus Wyeth owes them economic damages. The Fund asserts a derivative claim: It seeks to represent all third-party payers who have reimbursed these patients for Duraet.

Wyeth asked the district court to deny the motion to certify the class on the pleadings or, in the alternative, to allow class discovery and an evidentiary hearing. The plaintiffs agreed that discovery would be appropriate; accordingly, on November 28, 2000, the parties submitted a proposed discovery plan to the district court. That same day, despite the plaintiffs’ concession in favor of discovery, the court denied Wyeth’s request for discovery and an evi-dentiary hearing and certified the class under Fed.R.Civ.P. 23(b). 2

Even though Fed.R.CivP. 26(d) prohibits discovery and evidentiary hearings in advance of the pretrial conference, and the pretrial conference had been held only *318 thirteen days earlier, the district court rebuked Wyeth for not having pursued discovery over the past four months and decided it could certify the class without any discovery. Accordingly, although the record contained no evidence on Rivera’s purchase or use of Duract or on the Fund’s reimbursement of Duract patients, the court held that the claims of Rivera and the Fund “appear to be typical” of the class members.

Similarly, the district court dismissed Wyeth’s argument that variations in the fifty states’ laws would swamp any common issues. There was no need to analyze different states’ laws or even to decide which laws applied, the district court held, because plaintiffs had promised eventually to provide a workable subclass plan that would solve any problems.

Wyeth timely filed, and this court granted, an application for interlocutory appeal pursuant to rule 23(f). Apparently estimating that their odds on appeal were bleak, plaintiffs moved the district court to issue an order “expressing the court’s intent to vacate the class certification order and to reconsider the class certification issue upon remand.” The plaintiffs noted that the district court had erred in failing to conduct a choice-of-law analysis and failing to demand plaintiffs submit a subclass plan before certification; plaintiffs requested the court to assure that it would do so on remand; nonetheless, the court denied the motion on the stated ground of lack of jurisdiction.

III.

Rarely on appeal does the appellee concede that the district court’s order is so fatally flawed that it cannot stand. Yet, at oral argument, the attorney for Rivera and the Fund did just that, admitting that only a “feeling of obligation to support the district court order” moved him to argue when it was “crystal clear” we would have to vacate and remand. 3 Counsel was only half right, however: Because this suit does not even present a justiciable case or controversy under Article III, we vacate and render a judgment of dismissal.

IV.

Article III limits the judicial power of the federal courts to “Cases” and “Controversies” but does not define those terms. Instead, “the Constitution’s central mechanism of separation of powers depends largely upon common understanding of what activities are appropriate to legislatures, to executives, and to courts.” Lujan v. Defenders of Wildlife, 504 U.S. 555, 559-60, 112 S.Ct. 2130, 119 L.Ed.2d 351 (1992). An “essential and unchanging part” of this common understanding is the doctrine of standing. Id. at 560, 112 S.Ct. 2130.

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Rivera v. Wyeth-Ayerst Laboratories, 283 F.3d 315, 2002 WL 230657 (5th Cir. 2002).

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