Vaginal Mesh Lawsuit Against American Medical Systems Filed By Wright & Schulte LLC

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Vaginal Mesh Lawsuits Continue to Mount in State and Federal Litigations. Bellwether Trials Scheduled this Year

Wright &Schulte LLC offers free lawsuit evaluations to victims of transvaginal mesh injuries following implantation of transvaginal mesh. Visit www.yourlegalhelp.com, or call toll FREE 1-800-399-0795

Wright &Schulte LLC offers free lawsuit evaluations to victims of transvaginal mesh injuries following implantation of transvaginal mesh. Visit www.yourlegalhelp.com, or call toll FREE 1-800-399-0795

Wright &Schulte LLC offers free lawsuit evaluations to victims of transvaginal mesh injuries following implantation of transvaginal mesh. Visit www.yourlegalhelp.com, or call toll FREE 1-800-399-0795

Wright & Schulte LLC, an experienced defective medical device law firm, has filed a vaginal mesh lawsuit against American Medical Systems, Inc. on behalf of a Georgia woman who was implanted with the Monarc Subfascial Hammock in 2011. The Transvaginal Mesh Lawsuit was filed in the American Medical Systems, Inc., Pelvic Repair Systems Products Liability Litigation ( Vaginal mesh MDL No. 2325 ) now underway in U.S. District Court, Southern District of West Virginia, and includes vaginal mesh injury claims for Design Defect, Manufacturing Defect, Failure to Warn, Negligent Infliction of Emotional Distress and Gross Negligence, among others. (Case No. 2:13-cv-00199). Vaginal mesh lawsuits, also known as transvaginal mesh lawsuits or bladder mesh lawsuits continue to mount in other state and federal litigations

Wright & Schulte LLC is representing numerous plaintiffs in vaginal mesh lawsuits in the litigations underway in the Southern District of West Virginia. The Firm offers free vaginal mesh lawsuit or bladder mesh evaluations to victims of vaginal mesh injuries. If you or someone you love suffered serious, life-altering complication following implantation of transvaginal mesh, please visit yourlegalhelp.com, or call toll-FREE 1-800-399-0795 to learn more about your options for legal recourse.

Vaginal Mesh Devices and The FDA
Vaginal mesh devices are used in the surgical repair of pelvic organ prolapse and stress urinary incontinence. Most of the devices currently on the market were approved via the U.S. Food & Drug Administration’s (FDA) 510(K) approval process, which does not require human testing. In September 2011, an FDA advisory panel recommended that vaginal mesh used in pelvic organ prolapse repair be reclassified as a high-risk medical device, which would make them ineligible for 510(k) approvals. In January 2012, the FDA ordered the manufacturers of vaginal mesh products to conduct post-market safety studies of the devices to help the agency better understand their safety profile. This followed the issuance of a Safety Communication in July 2011 in which the FDA warned of the risk for vaginal mesh complications. At the time, the agency concluded that serious injuries associated with surgical mesh for transvaginal repair of pelvic organ prolapse, were “not rare,” and further advised that transvaginal prolapse repair with mesh “does not improve symptomatic results or quality of life over traditional non mesh repair.”
[[http://www.fda.gov/MedicalDevices/ProductsandMedicalProcedures/ImplantsandProsthetics/UroGynSurgicalMesh/default.htm

Vaginal Mesh Lawsuits Pending In Federal MDL's and State Courts
Thousands of women have since filed vaginal mesh lawsuits against American Medical Systems and other manufacturers. In addition to the American Medical Systems litigation, four other pelvic mesh litigations are underway in the Southern District of West Virginia, including:
In re: Boston Scientific Corp., Pelvic Repair System Products Liability Litigation (MDL No. 2326);
In re: C. R. Bard, Inc. Pelvic System Products Liability Litigation (MDL 2187);
In re: Ethicon, Inc., Pelvic Repair System Products Liability Litigation (MDL No. 2327); and
In Re: Coloplast Corp. Pelvic Support System Products Liability Litigation (MDL No. 2387).
According to court documents, the first of those trials will start next month, involving a C.R. Bard vaginal mesh device. Additional bellwether trials will begin in June.

Two additional consolidated transvaginal mesh litigations have also been established in New Jersey Superior Court, Bergen County, involving vaginal mesh devices manufactured by C.R. Bard and Ethicon Inc. The first trial in the New Jersey Ethicon litigation got underway this month, and is expected to conclude within a few weeks. (In re: Pelvic Mesh Litigation/Bard, No. L-6339-10 and In re Pelvic Mesh/Gynecare Litigation, No. 6341-10)

About Wright & Schulte LLC
Wright & Schulte LLC, an experienced personal injury firm, is dedicated to the belief that America’s legal system should work for the people. Every day, the attorneys of Wright & Schulte LLC stand up for the rights of people who have been injured or wronged by defective drugs and their side effects, complications from defective medical devices, and unsafe consumer products, and fight tirelessly to ensure that even the world’s most powerful corporations take responsibility for their actions. If you’re looking for a law firm that will guarantee the aggressive and personal representation you deserve, please do not hesitate to contact Wright & Schulte LLC today. Free Vaginal Mesh Lawsuit evaluations are available through yourlegalhelp.com, or call 1-800-399-0795.
Contact:
Wright & Schulte LLC
812 East National Road
Vandalia, Ohio 45377
1-800-399-0795

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