Model Number KNEE SCORPION |
Device Problem
Physical Resistance/Sticking (4012)
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Patient Problem
Insufficient Information (4580)
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Event Date 11/28/2023 |
Event Type
Injury
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Event Description
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On 11/28/2023, it was reported by a facility representative via sems-06411233 that an ar-12990 knee scorpion had a needle lodged in the shaft.This occurred during a case where the root repair could not be completed because the instrument could not be used.
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Manufacturer Narrative
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The contribution of the device to the reported event could not be determined as the device was not returned for evaluation.The root cause of the event could not be determined from the information available and without device evaluation.If the device becomes available for evaluation, a follow-up report will be submitted.
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Search Alerts/Recalls
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