In re Vioxx Products Liability Litigation

843 F. Supp. 2d 654, 2012 U.S. Dist. LEXIS 2526, 2012 WL 10552
CourtDistrict Court, E.D. Louisiana
DecidedJanuary 3, 2012
DocketMDL No. 1657
StatusPublished
Cited by12 cases

This text of 843 F. Supp. 2d 654 (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, 843 F. Supp. 2d 654, 2012 U.S. Dist. LEXIS 2526, 2012 WL 10552 (E.D. La. 2012).

Opinion

ORDER & REASONS

ELDON C. FALLON, District Judge.

Currently pending before the Court is the Commonwealth of Kentucky’s Motion to Remand (Rec. Doc. 63194). The Court has reviewed the briefs and the applicable law and heard oral argument on the motion and is now prepared to rule.

I. FACTUAL BACKGROUND AND PROCEDURAL HISTORY

To put this matter in perspective, a brief review of this litigation is appropriate. This multidistrict products liability litigation involves the prescription drug Vioxx, known generically as Rofecoxib. Merck, a New Jersey corporation, researched, designed, manufactured, marketed and distributed Vioxx to relieve pain and inflammation resulting from osteoarthritis, rheumatoid arthritis, menstrual pain, and migraine headaches. On May 20, 1999, the Food and Drug Administration approved Vioxx for sale in the United States. Vioxx remained publicly available until September 20, 2004, when Merck withdrew it from the market after data from a clinical trial known as APPROVe indicated that the use of Vioxx increased the risk of cardiovascular thrombotic events such as myocardial infarction (heart attack) and ischemic stroke. Thereafter, thousands of individual suits and numerous class actions were filed against Merck [656]*656in state and federal courts throughout the country alleging various products liability, tort, fraud, and warranty claims. It is estimated that 105 million prescriptions for Vioxx were written in the United States between May 20, 1999 and September 30, 2004. Based on this estimate, it is thought that approximately 20 million patients have taken Vioxx in the United States.1

California was the first state to institute a consolidated state court proceeding on October 30, 2002. New Jersey and Texas soon followed suit, on May 20, 2003 and September 6, 2005, respectively. On February 16, 2005, the Judicial Panel on Multidistrict Litigation (“MDL”) conferred MDL status on Vioxx lawsuits filed in various federal courts throughout the country and transferred all such cases to this Court to coordinate discovery and to consolidate pretrial matters pursuant to 28 U.S.C. § 1407. See In re Vioxx Prods. Liab. Litig., 360 F.Supp.2d 1352 (J.P.M.L. 2005). Additionally, a number of state and local governments filed suits against Merck seeking to recover amounts paid for Vioxx prescriptions on behalf of their citizens or civil penalties pursuant to state consumer protection statutes.

The Commonwealth of Kentucky, through Attorney General Jack Conway, filed one such action against Merck in the Circuit Court of Franklin County, Kentucky on September 28, 2009. Merck removed the case to the United States District Court for the Eastern District of Kentucky, asserting federal question jurisdiction under 28 U.S.C. § 1331 and diversity jurisdiction pursuant to the Class Action Fairness Act (“CAFA”), 28 U.S.C. § 1332(d). The case was transferred to this Court by the JPML on April 15, 2010.

On June 29, 2010, the Court issued Pretrial Order 39A and set a schedule for coordinated discovery in the pending Governmental actions, including Kentucky’s suit. The Court stayed discovery in the governmental cases on November 22, 2010 so that the parties could explore global resolution of the governmental actions. During the stay, counsel for the Commonwealth of Kentucky raised the issue of a briefing schedule on a motion to remand or transfer its case to Kentucky state court. At a status conference on August 4, 2011, the Court set a briefing schedule.

II. PRESENT MOTION

Kentucky has filed a motion to remand the case to Kentucky state court for lack of subject matter jurisdiction. With respect to diversity jurisdiction, the Commonwealth contends that the case is not a class action for the purposes of CAFA and that minimal diversity is lacking because Kentucky, the only named plaintiff, is not a citizen of itself. With respect to federal question jurisdiction, it argues that no federal question appears on the face of the complaint.

Merck opposes remand. It argues the case is functionally a class action for the purposes of CAFA jurisdiction and that the citizens of Kentucky supply the requisite diverse citizenship because they are the real parties in interest to some of the relief sought in the Complaint. Merck also argues that the Court has federal question jurisdiction over the case because the complaint implicates federal pharmaceutical laws and regulations.

III. LAW AND ANALYSIS

A. Standard on Motions to Remand

As the removing party, Merck has the burden of establishing federal ju[657]*657risdiction. Howery v. Allstate Ins. Co., 243 F.3d 912, 916 (5th Cir.2001). Removal jurisdiction “raises significant federalism concerns” and is strictly construed. Willy v. Coastal Corp., 855 F.2d 1160, 1164 (5th Cir.1988). Doubts regarding jurisdiction should be resolved against exercising jurisdiction. Acuna v. Brown & Root, Inc., 200 F.3d 335, 339 (5th Cir.2000).

The parties dispute whether the Court has either federal question jurisdiction pursuant to 28 U.S.C. § 1331 or diversity jurisdiction pursuant to 28 U.S.C. § 1332(d). In addressing a motion to remand for lack of federal question jurisdiction, the Court applies the “ Svell-pleaded complaint’ rule and searches for a federal question presented on the face of the complaint.” PCI Transp., Inc. v. Forth Worth & W. R.R. Co., 418 F.3d 535, 543 (5th Cir.2005).2 Likewise, the Court looks to the claims in the state court complaint at the time of removal to assess diversity jurisdiction. Manguno v. Prudential Prop. & Cas. Ins. Co., 276 F.3d 720, 723 (5th Cir.2002).

First, the Court will first set forth the allegations in the Commonwealth’s complaint which frame the jurisdictional arguments. Then, the Court will discuss why there is no diversity jurisdiction because this case is not a class action within the meaning of CAFA. Finally, the Court will discuss why no federal question appears on the face of the complaint.

B. The Commonwealth of Kentucky’s Complaint

The jurisdictional issues are framed by the allegations in Kentucky’s complaint. The complaint alleges a single count pursuant to the Kentucky Consumer Protection Act (“KCPA”).

Free access — add to your briefcase to read the full text and ask questions with AI

Related

Barone v. Bausch & Lomb, Inc.
372 F. Supp. 3d 141 (W.D. New York, 2019)
Hawaii Ex Rel. Louie v. HSBC Bank Nevada, N.A.
761 F.3d 1027 (Ninth Circuit, 2014)
Commonwealth ex rel. Conway v. Janssen Pharmaceuticals, Inc.
978 F. Supp. 2d 788 (W.D. Kentucky, 2013)
Erie Insurance Exchange v. Erie Indemnity Co.
722 F.3d 154 (Third Circuit, 2013)
Purdue Pharma L.P. v. Commonwealth of Kentucky
704 F.3d 208 (Second Circuit, 2013)
Mississippi ex rel. Hood v. AU Optronics Corp.
876 F. Supp. 2d 758 (S.D. Mississippi, 2012)
Merck Sharp & Dohme Corp. v. Conway
861 F. Supp. 2d 802 (E.D. Kentucky, 2012)

Cite This Page — Counsel Stack

Bluebook (online)
843 F. Supp. 2d 654, 2012 U.S. Dist. LEXIS 2526, 2012 WL 10552, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-vioxx-products-liability-litigation-laed-2012.