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Transvaginal Mesh Lawyers at Bernstein Liebhard LLP Note Upcoming Conference in New Jersey Pelvic Mesh Implant Lawsuits
Date:4/27/2013

sh erosion through vaginal tissue, infection, pain, urinary problems, and recurrence of prolapse and/or incontinence. The FDA also modified its previous position on the frequency of such complications, stating in the alert that injuries associated with pelvic organ prolapse repair were not rare. The following January, the agency ordered the manufacturers of mesh implant devices used in transvaginal prolapse repair to conduct post-market safety studies as part of its review. *

The nation’s first trial involving an Ethicon mesh product concluded in New Jersey state court in March, with the jury awarding more than $11 million in compensatory and punitive damages to the Plaintiff. Bernstein Liebhard partner, Jeffrey S. Grand, was a member of the trial team. (Gross v. Gynecare Inc., Atl-L-6966-10, Superior Court of Atlantic County, New Jersey (Atlantic City))

In addition to the mesh implant lawsuits pending in the New Jersey litigations, thousands of additional claims have been filed in consolidated proceedings now underway in U.S. District Court, Southern District of West Virginia, including: American Medical Systems, Inc., Pelvic Repair Systems Products Liability Litigation (“MDL No. 2325”); In re: Boston Scientific Corp., Pelvic Repair Systems Products Liability Litigation (“MDL No. 2326); In re: C.R. Bard, Inc., Pelvic Repair Systems Products Liability Litigation (“MDL No. 2187”); and In re: Ethicon, Inc., Pelvic Repair Systems Products Liability Litigation (“MDL No. 2327”). Mr. Grand is also serving on the Plaintiffs’ Steering Committee in these four proceedings.

Alleged victims of transvaginal mesh side effects may be entitled to compensation for their medical bills, pain and suffering, and other injuries. A wealth of information regarding mesh implant lawsuits can be found at Bernstein Liebhard's website. To learn more, please contact a transvaginal mesh lawyer today by calling 1-877-779-1414.

*fda.gov/MedicalDevices/Safe
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