Model Number N/A |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
No Code Available (3191)
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Event Type
Injury
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Event Description
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It was reported that patient underwent a hip procedure on an unknown date.Subsequently, a revision procedure has been indicated due to an unknown reason; however, no revision has been reported to date.
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Manufacturer Narrative
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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.Event is being reported to fda on one medwatch as the limited information available indicates that a revision may occur.Should additional information be received, the complaint will be reassessed and further medwatch reports will be submitted, if necessary.
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Manufacturer Narrative
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This follow-up report is being filed to relay initial reporter information, which was unknown at the time of the initial medwatch.
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Search Alerts/Recalls
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