| Catalog Number |
UKA-111-1111 |
| Health Effect - Clinical Code |
No Known Impact Or Consequence To Patient (2692)
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| Date of Event |
11/06/2017
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Type of Reportable Event
|
Malfunction
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Additional Manufacturer Narrative
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It was reported that the 8 mm poly insert would not fit into the tibial tray.The 6 mm poly insert was implanted to complete the case.Review of the device history record indicates that the device was manufactured to specification.
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Event or Problem Description
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It was reported that the 8 mm poly insert would not fit into the tibial tray.The 6 mm poly insert was implanted to complete the case.
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Search Alerts/Recalls
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