Catalog Number 113081 |
Device Problem
Device Displays Incorrect Message (2591)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 02/27/2019 |
Event Type
malfunction
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Manufacturer Narrative
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The patient's exact age is unknown; however, this was reported to be a pediatric patient.Should additional relevant information become available, a supplemental report will be submitted.
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Event Description
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It was reported that the blood in the extracorporeal circuit was not returned to the pediatric patient following a communication error (code 3) alarm on a prismaflex machine.This occurred during continuous veno-venous hemodiafiltration there was no report of patient injury or medical intervention associated with this event.No additional information is available.
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Manufacturer Narrative
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The device was not returned for evaluation.A service history review revealed no indication that the parts replaced during servicing caused or contributed to the reported event.Should additional relevant information become available, a supplemental report will be submitted.
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Search Alerts/Recalls
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