Model Number 5100060001 |
Device Problem
Failure to Auto Stop (2938)
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Patient Problem
Rupture (2208)
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Event Date 03/13/2023 |
Event Type
Injury
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Event Description
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It was reported that during a cranial procedure, the perforator bit did not stop spinning at the desired time.It was also reported that there was no medical intervention 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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H6: a follow up report will be filed once the quality investigation is complete.H3 other text : device not returned.
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Manufacturer Narrative
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H6: the quality investigation is complete.H2: no follow -up type as product not received to evaluate.H3 other text : device not returned.
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Event Description
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It was reported that during a cranial procedure, the perforator bit did not stop spinning at the desired time.It was also reported that there was no medical intervention 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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