The litigation over defective mesh products sold to women to treat pelvic organ prolapse (POP) and/or stress urinary incontinence (SUI) is among the largest in the history of pharmaceutical and medical device cases. More than 80,000 lawsuits have been filed in courts around the country.
Lawyers are the leaders in the fight for women around the country suffering from the adverse effects of the defective mesh products. Attorney’s have reached agreement in principle to settle claims for women implanted with defective mesh manufactured by the following entities:
Endo Pharmaceuticals (f/k/a American Medical Systems)
Coloplast • GMD
Attorneys are in active settlement negotiations with the remaining mesh manufacturers, but will continue to press forward with litigation until settlement is reached.)
If you or a loved one has been implanted with a pelvic mesh product and have experienced any adverse effects – pain, pain with intercourse, bleeding, new urinary dysfunction, erosion, surgery to remove the mesh, or anything else – the time to make a claim is now. There are limited time frames in which to participate in the settlements referenced above and limited time to file a lawsuit and preserve your right to participate in a settlement for the remaining manufacturers.
Contact us if you believe you have been injured as a result of a transvaginal mesh implant, even if you have not yet had a revision/removal surgery.