The patient¿s attorney alleged a deficiency against the device.The product was used for therapeutic treatment of a ventral incisional hernia.It was reported that after the implant, the patient experienced abscess, recurrence, adhesions, serosal tear, diathesis, staphylococcus aureus, and scarring.Post-operative patient treatment included revision surgery, incision/drainage of abscess, hernia repair with new mesh, lysis of adhesions, removal of suture material, wound packed, serosal tear repair, and removal of mesh.
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