In re Ephedra Products Liability Litigation

231 F.R.D. 167, 2005 WL 2179131
CourtDistrict Court, S.D. New York
DecidedSeptember 11, 2005
DocketNo. 04 M.D. 1598(JSR)
StatusPublished
Cited by7 cases

This text of 231 F.R.D. 167 (In re Ephedra Products Liability Litigation) is published on Counsel Stack Legal Research, covering District Court, S.D. New York primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In re Ephedra Products Liability Litigation, 231 F.R.D. 167, 2005 WL 2179131 (S.D.N.Y. 2005).

Opinion

OPINION

RAKOFF, District Judge.

On December 3, 2004, plaintiffs in Kline v. Metabolife International Inc., No. 04 Civ. 3351, and Westfall v. Metabolife International Inc., No. 04 Civ. 4255, moved for certification of a settlement-only class consisting of all persons in the United States who had ingested an ephedra-containing dietary supplement called “Metabolife 356” and for preliminary approval of a class settlement. Defendant Metabolife International Inc. (“Metabolife”) joined in that motion and moved separately for an injunction to stay 130 personal-injury actions commenced against Metabolife by members of the alleged class in the courts of many states. Both motions were vigorously opposed by the Plaintiffs’ Coordinating Counsel (“PCC”) and on April 7, 2005, Metabolife withdrew its motion for an injunction. As to the motion for certification of the settlement-only class and preliminary approval of the settlement, the Court, after receiving extensive written submissions and oral arguments, denied the motion by summary order dated June 2, 2005, with opinion to follow. This is that Opinion.

At the time of its denial of the motion, the Court had before it for consolidated pretrial proceedings about 300 ephedra products liability cases transferred here by the Judicial Panel on Multidistrict Litigation (the “MDL cases”), including some 170 eases against Me-tabolife (including Kline and Westfall).1 In addition, about 60 personal-injury actions against Twin Laboratories Inc. (a onetime manufacturer of ephedra products but unrelated to Metabolife) had been transferred here for trial from state and federal courts pursuant to 28 U.S.C. § 157(b)(5) and were consolidated for pretrial purposes with the MDL cases. Additionally, some 130 ephedra personal-injury cases were pending against Metabolife in various state courts. More than 90 of those were in California, where they had been consolidated for pretrial purposes under a state procedure similar to 28 U.S.C. § 1407.

Against this background, Klein and West-fall filed the instant motions for class certification and preliminary approval of the proposed settlement on December 3, 2004. At oral argument, Metabolife’s “settlement counsel” explained the genesis of the motion: Metabolife had retained him to craft a process for settling all 300 state-court and MDL cases involving Metabolife; he first approached the PCC with a proposal, but the PCC expressed a preference for settling cases individually; he then began negotiating with Klein and Westfall’s attorneys, who are not members of the PCC.2 See transcript, March 16, 2005, at 97-99,126; see also id. at 120-22. Counsel for Klein and Westfall explained that the negotiations were extensive; that they had retained one of the PCC’s experts, Christine Haller M.D., to evaluate the proposed matrix of injuries and compensation; and that with her assistance, they had reached settlement terms. See id. at 76.

As noted, Kline and Westfall’s notice of motion defines the class to be certified as all users of Metabolife 356 (the ephedra-contain-ing product) in the United States, as well as all persons having a derivative claim based on such use. Plaintiffs’ Motion for Preliminary Approval of Class Settlements ¶ 2. A class this broad might number millions, as, according to Metabolife, “Millions of people have consumed Metabolife’s ephedra-contain-ing products since 1995.” Metabolife’s Memorandum of Law on “Phase I” Briefing Issues Relating to Putative Class Settlement and All Writ Injunction at 1. Plaintiffs Kline and Westfall estimate, however, that the set[169]*169tlement class “consists of many thousands of persons — everyone in the United States who was injured by Metabolite’s ephedra products or sought treatment from a physician due to concerns about such injuries.” Plaintiffs’ Memorandum in Support of Motion for Preliminary Approval of Class Action Settlement at 13 (emphasis added). The difference is that the proposed settlement notice offers a “$250 Cash Medical Benefit” to users who suffered no injury but have “undergone medical screening by a health care professional in connection with their use” of Metabolite 356.

In any case, the number of users of Metabolite 356 who suffered significant personal injury is likely to be no more than a few hundred persons, ie., those already in litigation with Metabolite plus a few foreseeable latecomers. This is because a number of factors peculiar to ephedra make it likely that nearly all users of Metabolite 356 who suffered significant personal injury' — or their survivors — are already plaintiffs in the cases described above. Such factors include: (1) any injury from ephedra, as the experts agree, would manifest itself soon after ingestion (the proposed settlement here at issue set an outer limit of 21 days); (2) the Food and Drug Administration banned ephe-dra dietary supplements from the market in February 2004, so that the last colorable ephedra injuries occurred more than a year ago; (3) applicable statutes of limitations tend to be short, as little as one year in some relevant states; and (4) the risk of injury from ephedra has received broad public notoriety, making it unlikely that a user who suffered serious personal injury soon after taking ephedra would be unaware of the possible link and the potential for recourse to litigation.

Before turning to the merits of the instant motion, it should be noted that the Court did not review the proposed settlement for fairness because approval under Rule 23(e)(1)(C), Fed.R.Civ.P., was not sub judice. However, at least three procedural aspects of the proposed settlement were relevant to certification. First, the proposed settlement provided a matrix of ten “Injury Categories,” each having five possible levels of severity, yielding a total of 50 scheduled benefits. A benefit found in the matrix is then subject to reduction by percentages found in a “Confounding Factor Table,” where such factors as prior illness and smoking in various amounts are listed and further defined in 26 footnotes. Second, the proposed settlement provided a multilevel claims resolution procedure: a class member would submit a claim with documentation to a Claims Administrator, who would accept or disallow it; if it were allowed, Metabolite would have the right to demand an audit and interpose an objection; disputes between class members or Metabolite and the Claims Administrator would be referred for a hearing to a Special Master appointed by the Court upon approval of the settlement. Disputes were foreseeable over product identification, timing of symptoms, diagnosis, severity of injury, and confounding factors. Third, the proposed settlement gave Metabolite the right to “walk away” at any time up to twenty days after 50% of all registered claims had become final by exhaustion of the dispute procedure.

Turning then to the merits, the Court notes first that what the movants here initially sought was to have the Court in effect invent, purportedly under Rule 23 and the All Writs Act, an alternative to the Bankruptcy Code for granting Metabolite a stay of litigation and discharge of liability while affording only one class of potential creditors an equitable share of Metabolite’s limited assets. But even after the withdrawal of the stay motion, the proposed certification could not meet the requirements of Rule 23.

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Bluebook (online)
231 F.R.D. 167, 2005 WL 2179131, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-ephedra-products-liability-litigation-nysd-2005.