The patient¿s attorney alleged a deficiency against the device.The product was used for therapeutic treatment of an incisional hernia.It was reported that after underlay implant, the patient experienced mesh contraction, hematoma, abdominal wall mass, pain, adhesions, murky looking tissue, bulging, significant bleeding and was tachycardic.Post-operative patient treatment included blood transfusion, revision surgery.The device had been used with 31626 c-qur tacshield, lot# 410314005, exp date 2019-11-29.
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