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Transvaginal Mesh Lawyers at Wright & Schulte LLC Report on Recent Ruling Allowing Ohio Vaginal Mesh Lawsuit to Move Forward
Date:4/21/2013

complaint.

In its motion seeking dismissal, Boston Scientific asserted that the Plaintiff should have known in 2008 that her complications were allegedly the result of the Vesica transvaginal mesh product, and thus her claims were time barred. But Judge Carr did not agree, pointing out in his March 27th ruling that there was nothing in her lawsuit to suggest the Plaintiff “knew enough in 2008 to connect her occasional stress incontinence with the injuries that the device, according to her complaint, ultimately caused. Moreover, her doctor was, apparently, so unconcerned that he did nothing in response to her complaints.” Judge Carr also noted that “the multiple and severe symptoms that ultimately led to removal of the device did not manifest themselves until July, 2011.”

According to Wright & Schulte LLC, the Ohio transvaginal mesh lawsuit is just one of thousands of such claims pending against Boston Scientific and other medical device manufactures in courts around the country that have been filed on behalf of women who allegedly suffered serious vaginal mesh complications. Five consolidated litigations involving vaginal mesh lawsuits are currently underway in U.S. District Court, Southern District of West Virginia, including:

  •     In re: American Medical Systems, Inc., Pelvic Repair Systems Products Liability Litigation
        (MDL No. 2325)
  •     In re: Boston Scientific Corp., Pelvic Repair System Products Liability Litigation (MDL No.
         2326);
  •     In re: C.R. Bard, Inc., Pelvic Repair Systems Products Liability Litigation (MDL No. 2187)
  •     In re: Ethicon, Inc., Pelvic Repair System Products Liability Litigation (MDL No. 2327); and

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