Catalog Number 5100060001 |
Device Problem
Failure to Auto Stop (2938)
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Patient Problem
Abrasion (1689)
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Event Date 12/02/2016 |
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 has been reported that the safety stopping mechanism did not work on the cranial perforator bit.It was also reported that the perforator bit is continuing to go through the dura.It was further reported that there was no delay as a result of this event.
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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 has been reported that the safety stopping mechanism did not work on the cranial perforator bit.It was also reported that the perforator bit is continuing to go through the dura.It was further reported that there was no delay as a result of this event.
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Search Alerts/Recalls
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