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Mesh Lawsuit – Bellwether Cases Selected in Federal Litigation Underway for Ethicon Transvaginal Mesh Lawsuits, Bernstein Liebhard LLP Reports
Date:7/28/2013

age, and mesh erosion and shrinkage.

Transvaginal mesh devices and related complications have been the subject of two U.S. Food & Drug Administration (FDA) Public Safety Alerts since October 2008.* While Ethicon has never announced a mesh recall for any of the Gynecare products involved in the litigation, the company did announce in June 2012 that it would stop sales of some of those device due to commercial concerns.**

Ethicon is just one of several pelvic mesh manufacturers facing litigation over these devices in the Southern District of West Virginia. Bernstein Liebhard LLP partner, Jeffrey S. Grand, is also serving on the Plaintiffs’ Steering Committees for proceedings involving American Medical Systems, Inc. (MDL No. 2325) Boston Scientific Corp., (MDL No. 2326); and C.R. Bard, Inc., (MDL No. 2187). Court documents show that the first of the litigations’ bellwether trials, involving a C.R. Bard product, is scheduled to begin on July 29, 2013.

Mr. Grand has also been named Co-Liaison Counsel in two consolidated litigations established for C.R. Bard and Ethicon transvaginal mesh lawsuits that are currently underway in New Jersey’s Atlantic County Superior Court. He was also a member of the trial team on the first Ethicon trial in that proceeding, which ended in March with an $11 million verdict for the Plaintiff. (In re: Pelvic Mesh/Gynecare Litigation, No. 6341-10; In re: Pelvic Mesh Litigation/Bard, No. L-6339-10)

Women who have allegedly suffered serious complications associated with transvaginal mesh may be entitled to compensation for their medical bills, pain and suffering, and other injuries. A wealth of information regarding transvaginal mesh lawsuits is available at Bernstein Liebhard's website. To arrange for a free mesh lawsuit review with an experienced medical device attorney, please contact
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