Manufacturers of transvaginal mesh used to treat pelvic organ prolapse and stress urinary incontinence are being sued by tens of thousands of women who claim defective mesh caused internal injuries and left many in constant pain. Since the U.S. Food and Drug Administration (FDA) reclassified transvaginal mesh as a high-risk device earlier this year, acknowledging more than 1,500 reports of problems, these numbers are only likely to increase. According to the FDA, reported complications from the transvaginal placement of the surgical mesh include erosion of the mesh into the vaginal tissue, organ perforation, pain, infection, painful intercourse, and urinary and fecal ... Read More
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