Catalog Number 999890141 |
Device Problems
Nonstandard Device (1420); Noise, Audible (3273)
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Patient Problem
Pain (1994)
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Event Date 06/22/2017 |
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.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.The correction/removal reporting number listed applies to the corresponding product code sold domestically.
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Event Description
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Asr revision, asr xl: left, reason(s) for revision: implant noise and pain.
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Manufacturer Narrative
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Asr revision asr xl: left reason(s) for revision: implant noise and pain the reported event has been evaluated and will be monitored.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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