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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 03/23/2019 |
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 home patient (hp) experienced air in the patient line of a homechoice (hc) cassette, without an alarm.The hp was connected at the time of the event.This occurred during initial drain of peritoneal dialysis therapy.There was nothing unusual found during troubleshooting that would cause or contribute to the event.The hp stated that after they connected they saw an air gap in the patient line.Renal therapy services assisted the hp to end therapy, disconnect in the aseptic way and start over with all new supplies.There was no patient injury or medical intervention associated with this event.No additional information was available.
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Search Alerts/Recalls
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