Catalog Number UNK HIP FEMORAL STEM |
Device Problem
Biofilm coating in Device (1062)
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Patient Problems
Tissue Damage (2104); Test Result (2695)
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Event Type
Injury
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Manufacturer Narrative
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Product complaint : (b)(4).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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Ppf and sticker sheets received.Elevated metal ions after the first revision.Doi: (b)(6) 2012 - dor: not reported (left hip).
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Manufacturer Narrative
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Product complaint # (b)(4).This product was reported in error.No patient death, serious injury or evidence of reportable product malfunction occurred.Depuy considers the investigation closed at this time.Should any additional information be received to change the outcome of the performed investigation, the complaint will be re-opened.
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Search Alerts/Recalls
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