CareFusion 303, Inc. recalls Alaris Pump Module, Model No. 8100 and AIL sensor kits, P/N 147083-102 and P/N 49000221. The Alaris Pump module is a

Recalled January 25, 2017 · FDA recall Z-0950-2017 · CareFusion 303

Hazard

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

Units

382,635 units

Sold at

Nationwide Distribution

Description

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

Product

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 delivery through clinically acceptable routes of administration such as intravenous or epidural

Manufacturer(s)

CareFusion 303, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →