It was reported by the patient's attorney that as a result of having the product implanted, the patient has experienced injury, pain, discomfort, urinary problems, dyspareunia, additional surgeries, erosion and urinary incontinence.Product was used for therapeutic treatment.Per additional information received on 19nov2021, the patient has experienced vaginal mesh erosion, dyspareunia, hispareunia, recurrent stage 2 pelvic organ prolapse, defecatory dysfunction and required additional surgical and non-surgical interventions.
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