Catalog Number 5400007000 |
Device Problem
Unintended Power Up (1162)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 02/10/2016 |
Event Type
malfunction
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Event Description
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It was reported that during a surgical procedure at the user facility the device was causing a handpiece to run unintentionally.The procedure was completed successfully.No delay, no medical intervention and no adverse consequences were reported with this event.
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Manufacturer Narrative
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Follow-up report submitted to document device evaluation results.
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Event Description
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It was reported that during a surgical procedure at the user facility the device was causing a handpiece to run unintentionally.The procedure was completed successfully.No delay, no medical intervention and no adverse consequences were reported with this event.
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Search Alerts/Recalls
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