It was reported by the plaintiff's attorney that the plaintiff allegedly experienced pain, extrusion, infection, urinary problems, bowel problems, dyspareunia, neuromuscular problems, emotional distress and a product problem.It was also reported that the plaintiff experienced stage 3 vaginal vault prolapse, urinary retention, polyuria, frequency urination, dysuria, urgency, incomplete bladder emptying, urethral hypermobility, erosion, urinary tract infection, rectocele, vaginal pressure, urge to urinate and bladder neck obstruction.Additionally, the plaintiff underwent a revision surgery.The device was partially explanted.Furthermore, it was reported that the plaintiff died.The cause of death was reported as blunt force trauma to head and upper body.Related to manufacturer report #: 3011770902-2016-00335.
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