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Catalog Number ASKU |
Device Problems
Fluid/Blood Leak (1250); Hole In Material (1293)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 02/04/2018 |
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 there was a leak from the hole in the patient line during the set up for peritoneal dialysis therapy.The home patient (hp) explained that they had the machine all set up and lines primed, walked away and when they came back, there was solution all over the floor.The hp ended the 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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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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