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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 06/24/2019 |
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 patient experienced air in the patient line of a homechoice cassette without an alarm.This occurred during an unspecified phase of automated peritoneal dialysis therapy.The patient was connected at the time of the event.There was nothing unusual found during troubleshooting that would cause or contribute to the event.The care giver (cg) stated that the patient line was completely primed, no leak was seen on the lines or bags and all the connections were tight.Renal therapy services discussed continuous ambulatory peritoneal dialysis with the cg and proper procedures per the user manual were reviewed.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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