The product identification necessary to review manufacturing history was not provided.Current information is insufficient to permit a conclusion as to the cause of the event.The following sections could not be completed with the limited information provided.Expiration date - ni.Date implanted - ni.Manufacture date ¿ ni.Event is being reported to fda on one medwatch since the limited information available indicates that a revision procedure may be necessary.Should additional information be received regarding a revision procedure, the complaint will be reassessed and, if warranted, further medwatch reports will be submitted.This report is based on allegations set forth in plaintiff¿s complaint and the allegations contained therein are unverified.Remains implanted.
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Legal counsel for patient reported patient allegations of postoperative right knee pain, ambulation difficulties, and loss of mobility.No revision has been reported to date.This report is based on allegations set forth in plaintiff's complaint and the allegations contained therein are unverified.
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