Catalog Number M57220600220 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Unspecified Infection (1930)
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Event Date 07/01/2014 |
Event Type
Injury
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Event Description
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Pt with a unicondylar knee implant developed an infection.Revision surgery occurred to exchange the poly inserts.
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Manufacturer Narrative
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Pt with a unicondylar knee implant developed an infection.Revision surgery occurred to exchange the poly inserts.Review of the device history record indicates that the device was manufactured to spec.
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Search Alerts/Recalls
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