
On August 16, 2011, the United States Judicial Panel on Multidistrict Litigation “MDL Panel” created a new multidistrict litigation (“MDL”) for Darvocet, Darvon, and Propoxyphene products liability cases, finding that centralization of these cases is appropriate under 28 U.S.C. § 1407. The MDL Panel decided to centralize the cases in the Eastern District of Kentucky (Covington Division). With the consent of that court, the cases will be assigned to Judge Danny C. Reeves. Accordingly, the MDL Panel ordered transfer of the seventeen actions before it for consideration to the Eastern District of Kentucky (Covington Division).
Defendant
drug manufacturers and pharmaceutical companies opposed centralization of the cases. However, the Panel sided with the plaintiffs, who argued for centralization on the grounds that all of these cases share complex questions of fact concerning the safety of Darvocet, Darvon and Propoxyphene. According to the Panel, the cases share factual issues as to 1) whether Darvocet, Darvon, and other medications containing Propoxyphene were defectively designed and marketed, 2) which defendants manufactured, licensed, or sold Propoxyphene products during various times, and 3) whether defendants knew or should have known of the increased risk of cardiovascular injuries with these medications and failed to provide adequate warnings of them.
The MDL concerns cardiovascular injuries associated with Darvocet, Darvon and other medications containing Propoxyphene. However, the MDL Panel left open the question of what particular cardiovascular-related injuries are or are not appropriate for inclusion in this MDL.