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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 08/24/2023 |
Event Type
malfunction
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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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Event Description
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On (b)(6) 2023, it was reported by a distributor via sems that an ar-12990 knee scorpion¿ was not passing the needle.This occurred during a case, another one was brought in and the surgery went on as planned.
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Search Alerts/Recalls
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