The patient¿s attorney alleged a deficiency against the device.The product was used for therapeutic treatment of pelvic prolapse.It was reported that after the implant, the patient experienced pelvic pain, vaginal discomfort, dyspareunia, pelvic spams, recurrent cystocele, nodular indurated band of tissue, folded mesh, adhesions, and inflammation.Post-operative patient treatment included excision of vaginal mesh, removal of suture material, anterior colporrhaphy, uterosacral ligament vaginal vault suspension, diagnostic cystoscopy, and intraoperative ureteral catheter placement.
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