The FDA issued a public health notification regarding use of surgical mesh for the repair of pelvic organ prolapsed and stress urinary incontinence. Surgical mesh has caused severe complications in some patients.
The FDA has issued a public health notification regarding use of surgical mesh for the repair of pelvic organ prolapsed and stress urinary incontinence. Surgical mesh has caused severe complications in some patients. While a lawsuit is pending, surgical mesh is still being used. The FDA recommends physicians obtain specialized training and be aware of the potential risks, thoroughly inform patients of adverse risks, and monitor patients closely for complications.
