Catalog Number 999800756 |
Device Problem
Appropriate Term/Code Not Available (3191)
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Patient Problem
No Code Available (3191)
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Event Date 01/18/2018 |
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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Patient was revised to address elevated metal ions.Doi: unknown; dor: (b)(6) 2018; unknown hip.
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Manufacturer Narrative
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(b)(4).
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Manufacturer Narrative
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(b)(4).Investigation summary: this hip replacement platform was voluntarily recalled from the market and the product codes are now considered inactive.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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Manufacturer Narrative
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This is a duplicate report of 1818910-2013-02725.(b)(4) is being retracted as it is a report duplication. 1818910-2013-02725 will be kept for investigation purposes.
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Search Alerts/Recalls
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