Model Number 6000-011-000 |
Device Problem
Deformation Due to Compressive Stress (2889)
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Patient Problems
No Consequences Or Impact To Patient (2199); No Patient Involvement (2645)
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Event Date 11/25/2019 |
Event Type
malfunction
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Event Description
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It was reported that after a procedure in the sterile processing department at the user facility, the device's tip was found to be bent.A bent tip can lead to inaccuracies during a procedure.No medical intervention and no adverse consequences were reported with this event.As this event occurred after a procedure at the user facility, there was no delay to a surgical 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 after a procedure in the sterile processing department at the user facility, the device's tip was found to be bent.A bent tip can lead to inaccuracies during a procedure.No medical intervention and no adverse consequences were reported with this event.As this event occurred after a procedure at the user facility, there was no delay to a surgical procedure.
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Search Alerts/Recalls
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