FDA Issues Proposed Orders to Reclassify Transvaginal Mesh to a High-Risk Device

Ashley Brittain Landers of Schlichter, Bogard & Denton, LLP reports that the FDA has issued proposed orders to reclassify transvaginal mesh devices to the classification of high-risk. The attorneys at Schlichter, Bogard & Denton, LLP are offering free and confidential case reviews to those who allege to have suffered serious injuries associated with the use of transvaginal mesh (TVM) devices. St. Louis, MO (PRWEB) May 23, 2014 On April 29, 2014, the FDA issued an immediate release notifying the public that it has issued two proposed orders to address risks associated with surgical
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