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 implant, the patient experienced product failed, mesh migration, mesh contraction, adhesions to the vital structures including the spermatic cord, laceration of spermatic cord, hernia recurrence, mental/physical pain, inflammation, bowel necrosis, fistula, extensive bowel adhesions, bowel deserosalization, bowel erosion, enterotomy, suffering, disability, impairment, and loss of enjoyment of life.Post-operative patient treatment included nerve resection, vasectomy, mesh revision surgeries, hernia repair with mesh, small bowel resection, and removal mesh.
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