The patient¿s attorney alleged a deficiency against the device.The product was used for therapeutic treatment of a ventral hernia.It was reported that after the implant, the patient experienced seroma, infection, abdominal pain, recurrence, mesh migration, adhesions, inflammation, abscess, colon deseasonalized, and fluid collection.Post-operative patient treatment included drainage of fluid collection, partial removal of mesh, lysis of adhesions, abdominal wall reconstruction with bilateral sliding rectus abdominis myofascial, application of negative pressure wound dressing, and hernia repair with new mesh.
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