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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 06/04/2018 |
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 a patient experienced air in the patient line of a homechoice cassette without an alarm.This occurred during an unspecified step of peritoneal dialysis therapy, and on multiple occasions as far back as seven months ago.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.Renal therapy services advised the patient to perform continuous ambulatory peritoneal dialysis (capd) to complete the therapy.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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