Catalog Number 5100060001 |
Device Problem
Failure to Auto Stop (2938)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 04/13/2016 |
Event Type
malfunction
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Manufacturer Narrative
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A follow up report will be filed once the quality investigation is complete.
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Event Description
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It was reported that during a cranial procedure, the perforator bit failed to disengage.It is unknown if there were any adverse consequences and delays as a result of this event.No further information was provided.
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Manufacturer Narrative
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The definitive root cause could not be determined.Investigation results indicate that the returned device functioned as intended.
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Event Description
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It was reported that during a cranial procedure, the perforator bit failed to disengage.It is unknown if there were any adverse consequences and delays as a result of this event.No further information was provided.
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Search Alerts/Recalls
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