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Bernstein Liebhard LLP Launches New Transvaginal Mesh Lawsuit Website for Women Allegedly Injured by Pelvic Mesh Implants
Date:10/26/2013

U.S. on behalf of women allegedly injured by pelvic mesh implants. Many of these cases are currently pending in separate federal multidistrict litigations underway in the U.S. District Court, Southern District of West Virginia over products manufactured by C.R. Bard Inc., American Medical Systems Inc., the Johnson & Johnson subsidiary, Ethicon Inc., Boston Scientific Corp., and other companies. Bernstein Liebhard LLP partner, Jeffrey S. Grand, is currently a member of the Plaintiffs’ Steering Committees for the following four federal proceedings: American Medical Systems (MDL No. 2325), Boston Scientific Corp., (MDL No. 2326); C.R. Bard, Inc., (MDL No. 2187), and Ethicon, Inc. (MDL No. 2327).

In New Jersey’s Atlantic County Superior Court, Mr. Grand is also serving as Co-Liaison Counsel in two separate consolidated litigations established for lawsuits that allege injuries caused by pelvic mesh manufactured by Ethicon and C.R. Bard Inc. He was also an active member of the trial team in the Ethicon proceeding’s first trial, which concluded in March with an $11 million damage award to the Plaintiff. (In re: Pelvic Mesh/Gynecare Litigation, No. 6341-10; In re: Pelvic Mesh Litigation/Bard, No. L-6339-10)

The U.S. Food and Drug Administration (FDA) issued its first official vaginal mesh side effects warning in 2008, citing mesh erosion, organ damage, chronic infections and shrinkage as the most commonly reported transvaginal mesh complications.* At the time, the frequency for these injuries to occur was classified as “rare,” a stance the agency upgraded to “not rare” in 2011 after the number of FDA-filed complaint reports dramatically increased over a three-year period.

If you experienced pain during sexual intercourse, chronic infection, vaginal scarring or another injury after receivin
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