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Transvaginal Mesh Lawsuits Move Forward, as Bernstein Liebhard LLP Notes Release of New Order in Federal Ethicon Vaginal Mesh Litigation
Date:8/28/2013

New York, New York (PRWEB) August 28, 2013

Thousands of transvaginal mesh lawsuits (http://www.mesh-lawyers.net/) alleging serious injuries due to Ethicon Inc.’s Gynecare pelvic mesh products continue to move forward in a multidistrict litigation underway in U.S. District Court, Southern District of West Virginia, Bernstein Liebhard LLP reports. According to a Pretrial Order issued by the Court on August 26, 2013, procedures have been established for the selection of vaginal mesh lawsuits for the litigation’s first bellwether trials involving Gynecare Prolift devices. The first of those trials is scheduled to begin on August 19, 2014. (In re: Ethicon, Inc., Pelvic Repair Systems Products Liability Litigation - MDL No. 2327)

“Our Firm is representing numerous women who have suffered serious vaginal mesh complications, allegedly due to the defective nature of Gynecare Prolift mesh. We are pleased with the progress of this litigation,” says Bernstein Liebhard LLP, a nationwide law firm representing victims of defective drugs and medical devices. Firm partner, Jeffrey S. Grand, is serving on the Plaintiffs’ Steering Committee in the federal Ethicon litigation. Bernstein Liebhard LLP continues to evaluate transvaginal mesh lawsuits on behalf of women allegedly injured by pelvic mesh products marketed by Ethicon, Inc. and other manufacturers.

Ethicon Vaginal Mesh Lawsuits
Court documents indicate that more than 4,400 Ethicon transvaginal mesh lawsuits are currently pending in the Southern District of West Virginia. All of the claims allege that the company’s Gynecare pelvic mesh products were defectively designed and manufactured, and caused women to suffer serious vaginal mesh complications, including mesh erosion, scarring, and chronic pain and infection.

Vaginal mesh lawsuits have been mounting since October
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