The patient¿s attorney alleged a deficiency against the device.The product was used for therapeutic treatment of a hernia.It was reported that after the implant, the patient experienced failure of mesh, recurrence, pain, chronic inflammation, bowel necrosis, fistula, extensive bowel adhesion, bowel deserosalization, bowel erosion, enterotomy, defective mesh, mental pain, disability, impairment, loss of enjoyment of life, and adhesions.Post-operative patient treatment included revision surgery and bowel resection.
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