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 mental pain, pain, scarring, permanent impairment, loss of enjoyment of life, defective mesh, chronic inflammatory response, discomfort, recurrent hernia was protruding through the middle of the mesh and the mesh had also lost structural integrity.Post-operative patient treatment included surgical intervention, mesh removal and hernia repair with mesh.
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