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New Transvaginal Mesh Lawsuit in American Medical Systems Pelvic Mesh Litigation filed by Wright & Schulte LLP is Underway in West Virginia Federal Court
Date:1/19/2013

(also called exposure, extrusion or protrusion), pain, infection, bleeding, pain during sexual intercourse (dyspareunia), organ perforation, and urinary problems. There were also reports of recurrent prolapse, neuro-muscular problems, vaginal scarring/shrinkage, and emotional problems. At the time, the FDA warned that transvaginal mesh has no clear advantage over non-mesh methods for treating pelvic organ prolapse, and may even pose additional risks.
http://www.fda.gov/MedicalDevices/Safety/AlertsandNotices/ucm262435.htm

The FDA is currently considering a recommendation made by its Obstetrics-Gynecology Devices Panel in September 2011 to reclassify transvaginal mesh used in pelvic organ proplapse repair from Class II to Class III. As part of its review, the agency has asked the manufacturers of transvaginal mesh products to conduct post-market safety studies of to address concerns involving the effectiveness and safety of these devices.
http://www.fda.gov/MedicalDevices/ProductsandMedicalProcedures/ImplantsandProsthetics/UroGynSurgicalMesh/default.htm

Wright & Schulte LLC, a leading 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

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