Tag: regulatory updates

Mesh for Pelvic Organ Prolapse

MDP’s Take on FDA Decision to Halt Pelvic Mesh

Today the FDA released an announcement that orders manufacturers Boston Scientific and Coloplast to stop selling surgical mesh intended for transvaginal repair of pelvic organ prolapse (POP). Everyone at Medical Device Problems applauds this decision, but we feel it was not made soon enough. These mesh devices were on the market for over 20 years, … Continued