Catalog Number 5100004000 |
Device Problem
Unintended System Motion (1430)
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Patient Problem
No Patient Involvement (2645)
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Event Date 01/22/2014 |
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 was causing 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 was causing 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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Upon visual inspection, the device was found to have internally damaged wiring.The device was discarded by the manufacturer.
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Search Alerts/Recalls
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