The patient¿s attorney alleged a deficiency against the device.The product was used for therapeutic treatment of an inguinal hernia.It was reported that after the implant, the patient experienced mental pain, scarring, permanent impairment, loss of enjoyment of life, defective mesh, pain, discomfort, inflammation, small bowel obstruction, ischemia, edematous and attenuated tissues, adhesions, recurrence, mesh struck onto the peritoneum, and scrotal swelling.Post-operative patient treatment included revision surgery, hernia repair with mesh, and removal of mesh.
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