Catalog Number 6003-012-000 |
Device Problem
Bent (1059)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 02/23/2016 |
Event Type
malfunction
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Event Description
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It was reported that the tip of the device bent during a surgical procedure conducted at the user facility.No impact to the patient, delays, medical interventions or adverse consequences were reported with this event.
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Manufacturer Narrative
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Additional information: the reported event that the tip was bent was not confirmed through the visual inspection.It was observed that the pointer tip was broken off.Any physical impact to the pointer, can cause product damage or operational failure.
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Event Description
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It was reported that the tip of the device bent during a surgical procedure conducted at the user facility.No impact to the patient, delays, medical interventions or adverse consequences were reported with this event.
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Search Alerts/Recalls
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