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 04/10/2017 |
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 by customer.
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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 was no adverse consequences and no delays as a result of this event, 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 was no adverse consequences and no delays as a result of this event, the procedure was completed successfully.
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Search Alerts/Recalls
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