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 abdominal pain, hernia recurrence, rectus diastasis, pain/suffering, emotional distress, defective mesh, disability, impairment, loss of enjoyment of life, loss of care, mental pain, distress, and loss of comfort.Post-operative patient treatment included resection of skin and subcutaneous tissue, and mesh removal surgery.
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