Catalog Number UNK-HIP |
Device Problem
Appropriate Term/Code Not Available (3191)
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Patient Problems
Pain (1994); Joint Swelling (2356)
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Event Date 06/23/2015 |
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.No 510# number provided because this implant is sold internationally with different indications for use; it is currently sold in the us under a different part number.Complete product detail has not been received at this time.If further information is received a follow-up medwatch will be filed as appropriate.
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Event Description
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Pinnacle revision.Right hip.Reason for revision: pain, swelling, high cobalt levels.
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Manufacturer Narrative
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No device associated with this report was received for examination.Depuy considers the investigation closed at this time.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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