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CareFusion 303, Inc. recalls Alaris Pump SmartSite Infusion Set, Model No. 2420-0500. Used to administer fluid and medications through a needle or
Recalled December 30, 2015 · FDA recall Z-0445-2016 · CareFusion 303
Hazard
CareFusion is recalling the Alaris Pump Module SmartSite Infusion Set because the disconnection and leakage may occur during infusion. · FDA Class II
Units
1,445,180 units
Sold at
Worldwide Distribution-US (nationwide) and the countries of Canada, Australia, and New Zealand.
Description
CareFusion is recalling the Alaris Pump Module SmartSite Infusion Set because the disconnection and leakage may occur during infusion.
Product
Alaris Pump SmartSite Infusion Set, Model No. 2420-0500. Used to administer fluid and medications through a needle or catheter inserted into the patient's artery or vein.
Manufacturer(s)
CareFusion 303, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →