Catalog Number 123430000 |
Device Problem
Break (1069)
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Patient Problem
No Information (3190)
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Event Date 02/11/2014 |
Event Type
Injury
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Event Description
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Patient was revised to address implant fracture.
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Manufacturer Narrative
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The investigation is ongoing.Depuy will notify the fda of the results of this investigation once it has been completed.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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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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Manufacturer Narrative
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The device associated with this report was not returned.Review of the device history records and/or a lot specific complaint database search was not possible as the lot code required was not provided.Requests for additional investigational inputs were made in accordance with wi-7915 appendix a.No additional information was obtained.The investigation could not verify or identify any product contribution to the reported event with the information provided.Based on the inability to identify root cause, the need for corrective action was not indicated.Depuy considers the investigation closed.Should additional information be received, the information will be reviewed and the investigation will be re-opened as necessary.
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Search Alerts/Recalls
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