Catalog Number 150600005 |
Device Problem
Loss of or Failure to Bond (1068)
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Patient Problems
Not Applicable (3189); No Code Available (3191)
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Event Date 05/09/2018 |
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.
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Event Description
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Patient was revised to address subsidence and loosening of tibial component at the cement to implant interface.Cement manufacturer is competitor.Doi: (b)(6) 2017 dor: (b)(6) 2018; left knee.
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Manufacturer Narrative
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Product complaint : (b)(4) investigation summary : no device associated with this report was received for examination.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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