Catalog Number 122136052 |
Device Problem
Disassembly (1168)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 12/01/2017 |
Event Type
Injury
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Manufacturer Narrative
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Product complaint # (b)(64).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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Der states that patient's pinnacle cup was revised due to 59 degree high cup angle and liner disassociation.Cup, screw, liner and head were replaced with new.Stem remained implanted.Doi:(b)(6) 2017; dor: (b)(6) 2017.Affected side: left hip.
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Manufacturer Narrative
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(b)(4).Investigation summary: no device associated with this report was received for examination.A worldwide complaint database search found no other reported incident(s) against the provided product/lot combination(s) since release for distribution.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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