The patient¿s attorney alleged a deficiency against the device.The product was used for therapeutic treatment of a right direct and right femoral hernia.It was reported that after implant, the patient experienced abdominal pain, bulging, bowel issues, keloid scarring, pain, suffering, disability, impairment, loss of enjoyment of life, loss of care, loss of comfort, and distress.Post-operative patient treatment included revision surgery, excision of keloid scar, and trigger point kenalog injection.
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