Catalog Number 2296101421 |
Device Problem
Vibration (1674)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 05/29/2019 |
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.Awaiting device return.
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Event Description
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It was reported that during a procedure on the wisdom tooth, three burs made noise and was moving.It was also reported that there was a forty-five minute delay as a result of this event.It was further reported that there were no adverse consequences as a result of this event and the procedure was completed successfully.This report is for the first bur.
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Manufacturer Narrative
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The device was not returned for investigation.The quality investigation is complete.
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Event Description
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It was reported that during a procedure on the wisdom tooth, three burs made noise and was moving.It was also reported that there was a forty-five minute delay as a result of this event.It was further reported that there were no adverse consequences as a result of this event and the procedure was completed successfully.This report is for the first bur.
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Search Alerts/Recalls
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