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Catalog Number ASKU |
Device Problem
Device Operates Differently Than Expected (2913)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 06/05/2018 |
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 there was air in the patient line of a homechoice cassette without an alarm.This occurred during initial drain of peritoneal dialysis therapy.The patient was connected at the time of the event.The caregiver found there were two inches of air gaps in the patient line.During troubleshooting, nothing was found that could have caused the air in patient line.Renal therapy services (rts) advised the patient to start over with new supplies.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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