Catalog Number 5100060001 |
Device Problem
Failure to Auto Stop (2938)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 09/12/2016 |
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.Device discarded.
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Event Description
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It was reported that during a cranial procedure, the perforator bit did not stop.It was also reported that there were no delays and no adverse consequences as a result of this event.It was further reported that the procedure was completed successfully.
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Manufacturer Narrative
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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 did not stop.It was also reported that there were no delays and no adverse consequences as a result of this event.It was further reported that the procedure was completed successfully.
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Search Alerts/Recalls
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