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Catalog Number 0940000000 |
Device Problem
Sparking (2595)
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Patient Problem
No Patient Involvement (2645)
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Event Date 11/29/2018 |
Event Type
malfunction
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Event Description
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It was reported during testing at the user facility that the device was sparking.There was no patient involvement, no delay, no medical intervention, and no adverse consequences.
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Manufacturer Narrative
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Supplemental submitted documenting device evaluation.
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Event Description
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It was reported during testing at the user facility that the device was sparking.There was no patient involvement, no delay, no medical intervention, and no adverse consequences.
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Search Alerts/Recalls
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