FDA Releases Report Highly Critical of Vaginal Mesh Bladder Slings

FDA Releases Report Highly Critical of Vaginal Mesh Bladder Slings The FDA's July 13, 2011 published report recites complaints and warnings pertaining to the growing number of injuries sustained by women who have suffered severe complications relating to transvaginal mesh surgery. The independent investigation conducted by the New Jersey personal injury law firm of Mazie Slater Katz & Freeman indicates that vaginal mesh bladder sling products, primarily constructed of polypropylene, including but not limited to the Gynecare Prolift, Bard Avaulta, Boston Scientific Pinnacle and Upho
Contributor
About
PRWeb, a leader in online news and press release distribution, has been used by attorneys, law firms and more than 40,000 organizations