Catalog Number 4205000000L |
Device Problem
Unintended Power Up (1162)
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Patient Problem
No Patient Involvement (2645)
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Event Date 06/11/2015 |
Event Type
malfunction
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Event Description
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It was reported during service at manufacturer facility that the handpiece runs on its own without activation.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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Failure analysis is in progress; additional information will be submitted once the quality investigation is completed.
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Manufacturer Narrative
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The device is a loaner handpiece, it was repaired and placed back into stryker stock.
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Event Description
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It was reported during service at manufacturer facility that the handpiece runs on its own without activation.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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Search Alerts/Recalls
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