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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 09/06/2020 |
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 unspecified line of a homechoice cassette without an alarm.This occurred during use of peritoneal dialysis therapy.The patient was connected at the time of the event.During the troubleshooting, the patient noticed there was air within the cassette inside the tubing.The patient discontinued therapy and started 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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