Catalog Number UKA-111-1111 |
Device Problem
Device Operates Differently Than Expected (2913)
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Patient Problem
Pain (1994)
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Event Date 10/01/2016 |
Event Type
Injury
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Manufacturer Narrative
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It was reported that tibial implant overhang was observed during the primary procedure.The patient has continued pain following the primary procedure.A revision surgery is planned to convert the patient to a total knee replacement system.Review of the device history record indicates the device was manufactured to specification.
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Event Description
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It was reported that tibial implant overhang was observed during the primary procedure.The patient has continued pain following the primary procedure.A revision surgery is planned to convert the patient to a total knee replacement system.
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Search Alerts/Recalls
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