Catalog Number 5100060001 |
Device Problem
Unintended Movement (3026)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 06/11/2018 |
Event Type
malfunction
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Manufacturer Narrative
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Awaiting device evaluation.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 plunged.It was also reported that there was no adverse consequences as a result of this event.It was further reported that there was no surgical delay.No further information was provided.
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Manufacturer Narrative
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The perforator product reported involved with this event was returned for evaluation and the disengagement mechanism within the perforator was tested and functioned as intended.The reported failure of failure to disengage could not be confirmed.
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Event Description
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It was reported that during a cranial procedure, the perforator bit plunged.It was also reported that there was no adverse consequences as a result of this event.It was further reported that there was no surgical delay.No further information was provided.
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Search Alerts/Recalls
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