Model Number N/A |
Device Problem
Malposition of Device (2616)
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Patient Problem
No Information (3190)
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Event Type
Injury
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Manufacturer Narrative
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Current information is insufficient to permit a conclusion to the cause of the event.The product identification necessary to review manufacturing history was not provided.
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Event Description
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Two patients identified in the article were revised approximately ten years post-implantation due to the position of the cup being considered not acceptable for the prevention of dislocation postoperatively.
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Manufacturer Narrative
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This follow-up report is being filed to relay corrected information.
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Event Description
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Two patients identified in the article were revised approximately ten years post-implantation.During the liner exchange, the shell was also revised because the position of the cup being considered not acceptable for the prevention of dislocation postoperatively.
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Search Alerts/Recalls
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