FDAFebruary 4, 2020device

CareFusion Alaris Syringe Module, Model 8110

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

1)Error 255-XX-XXX results in inability to edit settings 2)Delay options programming may result in no KVO rate/therapy interruption 3)Software errors results in no low battery alarm/infusion stopping 4)Medium priority KVO/End of Infusion alarms may result in unrecognized infusion completion 5)Custom concentration data entry errors results in concentrations being lower/higher than medication orders

What to do

FDA enforcement status: Ongoing

Brands named

carefusion 303carefusion

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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