Catalog Number 150600004 |
Device Problem
Loss of or Failure to Bond (1068)
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Patient Problem
No Information (3190)
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Event Date 07/25/2017 |
Event Type
Injury
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Manufacturer Narrative
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If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
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Event Description
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The patient was revised to address loosening of the tibial component at the cement to implant interface.Depuy cement was used.Update july 25, 2017: medical records have been reviewed and have been determined to have no new information.Reportability remains unchanged.Updated 8-14-2017.
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Manufacturer Narrative
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The device associated with this report was not received for examination depuy considers the investigation closed.Should additional information be received, the information will be reviewed and the investigation will be re-opened as necessary.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
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Search Alerts/Recalls
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