Catalog Number 5100004000 |
Device Problem
Device Remains Activated (1525)
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Patient Problem
No Patient Involvement (2645)
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Event Date 02/27/2014 |
Event Type
malfunction
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Event Description
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It was reported that during routine maintenance conducted by a manufacturer field service technician at the user facility the tps handpiece cord caused the handpiece to run on.It was reported that there was no associated procedure.No patient involvement, no delay, no medical intervention and no adverse consequences were reported with this event.
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Event Description
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It was reported that during routine maintenance conducted by a manufacturer field service technician at the user facility the tps handpiece cord caused the handpiece to run on.It was reported that there was no associated procedure.No patient involvement, no delay, no medical intervention and no adverse consequences were reported with this event.
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Manufacturer Narrative
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A follow up report will be filed after the quality investigation has been completed.
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Manufacturer Narrative
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During the device evaluation, the engineer determined the cable had internally damaged wiring as no external damage was found.The device was discarded by the manufacturer.
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Search Alerts/Recalls
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