Coloplast is one of more than 30 manufacturers of vaginal mesh responsible for putting millions of women at risk. Transvaginal mesh (TVM) is used to treat pelvic organ prolapse (POP) and stress urinary continence (SUI), and Bloomberg reports that one manufacturer indicated that more than a million women have had mesh implanted over the past 15 years. 
Unfortunately, vaginal mesh can begin to erode in the body and can fail to work as required for women. The mesh can cause women to experience significant pain, including discomfort during sexual intercourse. Vaginal mesh may also not be effective in treating POP, as many women experience recurrent prolapse of pelvic organs. Because of the myriad problems identified with vaginal mesh, the Food and Drug Administration issued an order in 2012 requiring manufacturers of mesh products to conduct studies to identify the rates of complications. These studies should assess how likely it is that the mesh will cause organ damage and other serious health problems.
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