Catalog Number 2C7462 |
Device Problem
Failure to Infuse (2340)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 07/18/2017 |
Event Type
malfunction
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Manufacturer Narrative
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(b)(4).The device has been received and the evaluation is in progress.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 clearlink system secondary medication set was not infusing.The patient was to be infused with (b)(6) of vancomycin connected to secondary tubing with 250ml bag of saline connected to the primary bag.The unspecified pump was set to infuse the vancomycin attached to the secondary tubing, but the patient was only infused with the normal saline attached to the primary tubing.The tubing was replaced.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 sample was received for evaluation.Functional testing was performed with no issues noted.The sample set primed and flow was normal.Visual inspection did not identify any abnormalities that could have contributed to the reported condition.A batch review was conducted and there were no deviations found related to this reported condition during the manufacture of this lot.The reported condition was not verified.Should additional relevant information become available, a supplemental report will be submitted.
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Search Alerts/Recalls
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