FDADecember 2, 2016device

Alaris Pump Module, Model No. 8100 and AIL sensor kits, P/N 147083-102 and P/N 49000221. The Alaris Pump module is a large volume infusion pump offered under the Alaris System. The Alaris Pump module will deliver medication and fluids using IV administration sets for continuous or intermittent de...

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

The hazard

During an infusion, a false Air-in-Line (AIL) alarm would cause the infusion to be interrupted.

What to do

FDA enforcement status: Terminated

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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