It was reported that patient underwent total hip arthroplasty on (b)(6) 2007.Subsequently, a revision procedure was performed on (b)(6) 2015 due to pain and instability.The product identification necessary to review manufacturing history was not provided.Event is being reported to fda on one medwatch since the limited information available indicates that a revision procedure occurred.Should additional information be received regarding the revision procedure, the complaint will be reassessed and, if warranted, further medwatch reports will be submitted.
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