Catalog Number 2C8541 |
Device Problems
Filling Problem (1233); Material Twisted/Bent (2981)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 01/03/2023 |
Event Type
malfunction
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Manufacturer Narrative
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Device manufacturer address 1: 1416980-2023-00287 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 tubing of an unspecified quantity of clearlink system continu-flo solution sets were kinked.This resulted in the drip titration not matching the expected response which led to additional medications being ordered in order to achieve the desired response.This issue occurred during 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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H10: 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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