Catalog Number 6000-011-000 |
Device Problem
Bent (1059)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 03/21/2018 |
Event Type
malfunction
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Event Description
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It was reported that during use the tip was bent.The tip being bent during a procedure can lead to inaccuracies and potential patient harm.There was no known patient impact, medical intervention, or delay to the procedure.
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Manufacturer Narrative
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Device evaluation: follow-up report submitted to document device evaluation results.
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Event Description
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It was reported that during use the tip was bent.The tip being bent during a procedure can lead to inaccuracies and potential patient harm.There was no known patient impact, medical intervention, or delay to the procedure.
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Search Alerts/Recalls
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