It was reported by the plaintiff's attorney that the plaintiff allegedly experienced emotional distress and a product problem.It was also reported that the plaintiff experienced pain, pelvic inflammation, urinary tract infection, erosion, ventral hernia, adhesions, and bowel obstruction.In addition, the plaintiff underwent a series of removal surgeries; the device was partially explanted.Furthermore, it was reported that the plaintiff died.The causes of death were reported as cerebrovascular infarction, atrial fibrillation, anemia, hypertension and chronic kidney disease.
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