It was explained through the filing of a lawsuit that allegedly after implantation the patient began experiencing discomfort in the area of his device, initial diagnostic workup revealed gross failure of the lift anatomic v40 femoral head and marked elevation of serum cobalt, chromium and titanium.It is further alleged that as a result the patient was forced to have the device surgically removed and upon removal "it was apparent the device had failed causing gross deformation of the accolade tmzf stem together with severe and permanent tissue and muscle damage".
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