In Re Vioxx Products Liability Litigation

557 F. Supp. 2d 741, 2008 WL 2229264
CourtDistrict Court, E.D. Louisiana
DecidedMay 30, 2008
DocketMDL 1657
StatusPublished
Cited by27 cases

This text of 557 F. Supp. 2d 741 (In Re Vioxx Products Liability Litigation) is published on Counsel Stack Legal Research, covering District Court, E.D. Louisiana primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In Re Vioxx Products Liability Litigation, 557 F. Supp. 2d 741, 2008 WL 2229264 (E.D. La. 2008).

Opinion

ORDER & REASONS

ELDON FALLON, District Judge.

THIS DOCUMENT RELATES TO ALL CASES.

Before the Court are Certain Plaintiffs’ Emergency Motion for Modification and/or Suspension of Pre-Trial Order No. 28 (Rec. Doc. 14157). For the following reasons, the motion is GRANTED IN PART and DENIED IN PART.

1. BACKGROUND

On November 9, 2007, the parties announced the establishment of a Vioxx Resolution Program that encompasses all claims that allege a heart attack, sudden cardiac death, or stroke. Also on that date, the Court entered two pre-trial orders requiring Plaintiffs to provide certain information to Merck by certain deadlines. Pre-Trial Order No. 28 (“PTO 28”) requires all plaintiffs and tolling agreement claimants with claims pending as of November 9, 2007, to produce specified information regarding their claims if they are not eligible for or have not submitted their claims to the Vioxx Resolution Program. 1 PTO 28 requires that plaintiffs and tolling agreement claimants provide a case specific expert report to Merck by certain dates based on the plaintiffs’ last name. 2 Cases where the Plaintiffs last name begins with A through L must submit this information by May 1, 2008, and those Plaintiffs whose last names begin with L through Z must submit this information by July 1, 2008.

Certain Plaintiffs have filed a motion to suspend or modify the requirements of Pre-Trial Order 28. Plaintiffs argue that the requirement of PTO 28 to provide case specific expert reports is premature for those plaintiffs who allege injury related to thromboembolic disorders because the PSC has not yet developed general eausa *743 tion expert reports on this topic. For those plaintiffs who have an otherwise eligible claim but who elect not to participate in the Vioxx Settlement Program, Plaintiffs argue that PTO 28 does not provide them sufficient time to develop their case and/or seek new counsel. The Plaintiffs generally argue that PTO 28 is “unfair and unilaterally slanted in favor of Merck, both in general and specific application.”

Merck opposes Plaintiffs’ motion. First, Merck argues that orders such as PTO 28 have been endorsed by the Fifth Circuit and are a useful tool in mass tort proceedings. Merck states that PTO 28 is merely an “effort by the Court to manage an extremely large docket of complicated cases by requiring basic information about usage, injury, and causation.” Further, Merck argues that PTO 28 already contemplates extensions of time for “good cause” which will not prejudice Plaintiffs who elect not to participate in the Settlement.

The Court held a telephone conference with Merck and Plaintiffs’ counsel who filed the motion, and extended the deadline to file case specific expert reports until the next scheduled monthly status conference on May 22, 2008. The Court also instructed the PSC to add this motion as an agenda item for the monthly status conference and directed the PSC to provide its position on this motion. On May 22, 2008, the Court heard further argument on this matter. Following the monthly status conference, the Court issued an Order declining to extend the deadline further for Plaintiffs whose last names begin with A through L, however, the Court did state that it would not consider any motions to dismiss claims for failure to comply with this requirement until after July 23, 2008. The Court now takes the opportunity to reconsider the issue.

II. LAW & ANALYSIS

The type of pre-trial order at issue' is commonly known as a Lone Pine order. This name comes from Lore v. Lone Pine Corp. in which the Superior Court of New Jersey approved of a pretrial order requiring plaintiffs to provide some basic facts in the form of expert reports or run the risk of having their case dismissed. See 1986 WL 637507, *1-*3 (N.J.Super. Nov. 18, 1986). Lone Pine orders “are designed to handle the complex issues and potential burdens on defendants and courts in mass tort litigation.” Acuna v. Brown & Root, Inc., 200 F.3d 335, 340 (5th Cir.2000). “The basic purpose of a Lone Pine order is to identify and cull potentially merit less claims and streamline litigation in complex cases.” Baker v. Chevron USA, Inc., 2007 WL 315346, *1 (S.D.Ohio Jan.30, 2007). Since the New Jersey court’s decision, Lone Pine orders have been routinely used by courts to manage mass tort cases. See, e.g., Acuna, 200 F.3d at 340; Burns v. Universal Crop Protection Alliance, 2007 WL 2811533 (E.D.Ark. Sep.25, 2007); Baker, 2007 WL 315346; In re Rezulin Products Liability Litigation, 441 F.Supp.2d 567, 570 (S.D.N.Y.2006); In re Silica Products Liability Litigation, 398 F.Supp.2d 563, 576 (S.D.Tex.2005). 3

The United States Court of Appeals for the Fifth Circuit has recognized the value of and approved the use of Lone Pine *744 orders in mass tort litigation. In Acuna v. Brown & Root, Inc., the Fifth Circuit held that the district court was within its discretion to issue a scheduling order that “essentially required that information that plaintiffs should have had before filing their claims pursuant to Fed.R.Civ.P. 11(b)(3).” Acuna, 200 F.3d at 340. See also, Steering Comm. v. Exxon Mobil Corp., 461 F.3d 598, 604 (5th Cir.2006).

In crafting a Lone Pine order, a court should strive to strike a balance between efficiency and equity. Lone Pine orders may not be appropriate in every case and, even when appropriate, they may not be suitable at every stage of the litigation. For example, in the present case, a Lone Pine order may not have been appropriate at an earlier stage before any discovery had taken place since little was known about the structure, nature and effect of Vioxx by anyone other than perhaps the manufacturer of the drug. But this case is no longer in its embryonic stage. It has existed in state courts for over seven years and in this Court for over three years, and much discovery has taken place. In this MDL, the Plaintiffs’ Steering Committee (“PSC”) has established and organized a document depository to house materials produced by Merck and has made those materials available to Plaintiffs’ counsel in individual cases. In total, Merck has produced over 22 million pages of documents. Hundreds of depositions have taken place. This Court has ruled on approximately one thousand pretrial motions and has reviewed over 500,-000 pages of documents claimed to be subject to attorney-client privilege. Monthly status conferences, at which liaison counsel reported on all developments in the case, have been held in open court since the inception of this MDL.

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557 F. Supp. 2d 741, 2008 WL 2229264, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-vioxx-products-liability-litigation-laed-2008.