It was reported by the plaintiff's attorney that the plaintiff experienced recurrence of mixed urinary incontinence and vaginal vault prolapse, cystocele, rectocele, hypermobile urethra, failed mesh, urinary hesitancy, incomplete bladder emptying, vaginal atrophy, bladder and suprapubic pain, dysuria, urgency, frequency, nocturia, vulvar irritation, vaginal discharge and pyuria.It was also reported that the plaintiff allegedly experienced infection, organ perforation, bleeding, dyspareunia and vaginal scarring.The plaintiff underwent revision and the device was partially explanted.Furthermore, it was reported that the plaintiff died.The causes of death were reported as sepsis, aspiration pneumonia and dementia.Related to manufacturer report #: 3011770902-2016-00362.
|