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Mesh Lawsuit News: Bernstein Liebhard LLP Notes New Order in Federal Ethicon Vaginal Mesh Lawsuits
Date:7/29/2013

s Ethicon unit are also named defendants in more than 4,360 mesh lawsuits pending in a multicounty litigation underway in New Jersey’s Atlantic County Superior Court. C.R. Bard faces just over 800 claims filed in a second consolidated proceeding pending before the same judge. Mr. Grand has been named Co-Liaison Counsel in both litigations, and was a member of the trial team for the first Ethicon trial that concluded 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)

Mesh lawsuits have been mounting since October 2008, when the U.S. Food and Drug Administration (FDA) alerted the public that it had received more than 1,000 reports of serious vaginal mesh complications. In July 2011, the FDA issued a second alert, warning that the frequency of complications associated with transvaginal prolapse repair was “not rare.” While none of the manufacturers named in the ongoing litigation has issued a mesh recall in response to the FDA warning, Ethicon did announce in June 2012 that it would stop sales of some of its Gynecare devices due to commercial concerns.

Alleged victims of 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 vaginal mesh lawsuits is available at Bernstein Liebhard's Tranvaginal Mesh Lawsuit Center. To arrange for a free review of your mesh lawsuit, please contact the Firm today by calling 800-511-5092

*fda.gov/MedicalDevices/ProductsandMedicalProcedures/ImplantsandProsthetics/UroGynSurgicalMesh/default.htm
**bloomberg.com/news/2012-06-04/j-j-tells-judge-it-will-stop-selling-vaginal-mesh-implant.html

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