Catalog Number 5100060001 |
Device Problem
Failure to Auto Stop (2938)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 10/02/2017 |
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.Product status unavailable.
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Event Description
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It was reported that during a cranial procedure, the perforator bit did not stop.No further information was provided.
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Manufacturer Narrative
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The reported event, for perforator bit failure to disengage, was not confirmed as the perforator bit was not returned for evaluation.Without the perforator bit, the root cause cannot be determined.The quality investigation is closed.Product unavailable for return.
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Event Description
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It was reported that during a cranial procedure, the perforator bit did not stop.No further information was provided.
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Search Alerts/Recalls
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