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Transvaginal Mesh Lawsuit News: Bernstein Liebhard LLP Notes New Order in American Medical Systems Multidistrict Litigation
Date:7/17/2013

t scheduled to begin in December.

Separate multidistrict litigations are also underway in the Southern District of West Virginia for claims involving other mesh manufacturers, including: Boston Scientific Corp., (MDL No. 2326); C.R. Bard, Inc., (MDL No. 2187), and Ethicon, Inc. (MDL No. 2327). Bernstein Liebhard LLP partner, Jeffrey S. Grand, is also serving on the Plaintiffs’ Steering Committees for these proceedings.

Transvaginal mesh is used to surgically treat pelvic organ prolapse and stress urinary incontinence. In October 2008, the U.S. Food & Drug Administration (FDA) warned the public that it had received more than 1,000 reports of serious complications associated such devices over a three year period.* In July 2011, the FDA warned that vaginal mesh complications associated with prolapse repair had grown five-fold since its previous alert, and stated that it no longer considered these types of injuries to be rare.**

Hundreds of transvaginal mesh lawsuits have also been filed in state courts throughout the country. Mr. Grand is serving as 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 allegedly suffered serious complications due to transvaginal mesh, including chronic pain, infections, organ damage, and mesh erosion and shrinkage, may be entitled to file a surgical mesh lawsuit. A wealth of information regarding the transvaginal mesh litigation is available at Bernstein Liebhard's website. To arrange for a free legal consultation with an experienced

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