Catalog Number 129433125 |
Device Problem
Loss of or Failure to Bond (1068)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 12/21/2017 |
Event Type
Injury
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Manufacturer Narrative
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(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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The patient was revised to address loosening of the tibial component at the cement to implant interface, competitor cement was used.Doi: (b)(6) 2012; dor: (b)(6) 2017; left knee.
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Manufacturer Narrative
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This is a duplicate report of 1818910-2018-51156.Mfr report 1818910-2018-51161 is being retracted as it is a report duplication.Mfr report 1818910-2018-51156 will be kept for investigation purposes.
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Search Alerts/Recalls
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