Catalog Number ASKU |
Device Problems
Obstruction of Flow (2423); Device Displays Incorrect Message (2591)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 04/11/2019 |
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 unspecified access set was occluded causing an alarm on an unspecified pump.The set had a "fixed collar" that was connected to a one-link.When the set was disconnected the infusion ran; when connected the line occluded.The one-link was removed and line was patent, the one-link was flushed and it was patent.This was noted during product use.There was no report of patient injury or medical intervention associated with this event.No additional information is available.
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Manufacturer Narrative
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Additional information : 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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