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Catalog Number ASKU |
Device Problems
Cut In Material (2454); Device Displays Incorrect Message (2591)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 04/24/2018 |
Event Type
malfunction
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Manufacturer Narrative
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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 homechoice device experienced a system error 2240 (air in line/set) alarm.The patient was not connected at the time of the alarm.This occurred during drain three of four of peritoneal dialysis therapy.During troubleshooting, the caregiver reported that the catheter was cut in half.Renal therapy services guided the caregiver on removing the supplies and advised to contact the peritoneal dialysis registered nurse.There was no patient injury or medical intervention associated with this event.No additional information is available.
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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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Search Alerts/Recalls
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