Catalog Number ASKU |
Device Problems
Disconnection (1171); Fluid/Blood Leak (1250); Improper or Incorrect Procedure or Method (2017)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 06/10/2019 |
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 the patient line from a homechoice cassette disconnected from the patient line extension which resulted in a leak.This event occurred during fill one of peritoneal dialysis (pd) therapy.The patient was connected for pd therapy at the time of the event.It was further reported that the patient had not properly tightened the connection between the patient line and patient line extension.The technical service representative assisted the patient with ending the therapy and removing the supplies.The patient would restarted therapy with all 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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