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Model Number KNEE SCORPION |
Device Problem
Failure to Advance (2524)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 01/29/2024 |
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 1/29/2024, it was reported by a sales representative via (b)(4) that an ar-12990 knee scorpion would not feed the needles through.The case was completed by swapping for another device with no adverse effects on the patient.This was discovered during an unspecified procedure, with no reported patient harm.
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Search Alerts/Recalls
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