Model Number ACL TIGHTROPE WITH FIBERTAG |
Device Problem
Material Twisted/Bent (2981)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 01/05/2024 |
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 01/05/2024, it was reported by a distributor via email that an ar-1588rtt tightrope had a knot in the assembly.This occurred during use in a case with no patient effect.
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Search Alerts/Recalls
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