Catalog Number 4100126000 |
Device Problem
Component Missing (2306)
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Patient Problem
No Patient Involvement (2645)
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Event Date 12/08/2014 |
Event Type
malfunction
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Event Description
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It was reported that during equipment testing conducted by a manufacturer service technician that the c-clip was missing.No patient involvement, no clinically significant 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.Evaluation conclusion: the device has been discarded by the manufacturer.
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Event Description
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It was reported that during equipment testing conducted by a manufacturer service technician that the c-clip was missing.No patient involvement, no clinically significant delay, no medical intervention and no adverse consequences were reported with this event.
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Search Alerts/Recalls
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