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Catalog Number ASKU |
Device Problem
Improper Flow or Infusion (2954)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 11/16/2020 |
Event Type
malfunction
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Manufacturer Narrative
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The device was not returned and the lot number is unknown; therefore, a device analysis could not be completed.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 a patient experienced air in the patient line of a homechoice cassette without an alarm.This occurred during priming for peritoneal dialysis therapy.The patient was not connected at the time of the event.Renal therapy services assisted the patient with re-priming and connecting for therapy; however, the air bubbles were still observed at the patient line.There was nothing unusual found during troubleshooting that would cause or contribute to the event.Renal therapy services assisted the patient with ending the therapy session.There was no patient injury or medical intervention associated with this event.No additional information is available.
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Search Alerts/Recalls
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