Catalog Number 5C5479 |
Device Problem
Improper Flow or Infusion (2954)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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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 patient experienced air in the patient line of a homechoice cassette.This occurred during initial drain of peritoneal dialysis therapy.The home patient (hp) was connected at the time of the event.There was nothing unusual found during troubleshooting that would cause or contribute to the event.The patient reported that they successfully primed the set; however, during initial drain, it was observed that air bubbles were in the patient line.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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Manufacturer Narrative
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Correction: b4/f8: date of this report in the initial mdr is being corrected from blank to (b)(6) 2021.
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Search Alerts/Recalls
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