Initial communication received from the patient about this event did not include specific information about the implant (size and lot number).Likewise, no contact information for the implanting surgeon was provided.Product information, the physician's name and contact information, and details surrounding the reported event as described were not made available for investigation.As a result, a review of the quality and manufacturing records for the involved device (implant) lot could not be carried out, nor a patient impact assessment could be performed.At the present time, the event could not be definitely confirmed.Should additional details be provided in the future, an update to this submission will be provided.
|