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CareFusion 303, Inc. recalls Alaris Extension Sets with microbore tubing Model 20022 and 30914 Is used to administer fluid and medications from a
Recalled June 13, 2018 · FDA recall Z-2111-2018 · CareFusion 303
Hazard
Reports of incorrect priming volume due to manufacturing with incorrect tubing. · FDA Class II
Units
25,400 units
Sold at
US Distribution to states of: CA, IL, IN, KS, NE, NJ, TX, UT, VA and WA
Description
Reports of incorrect priming volume due to manufacturing with incorrect tubing.
Product
Alaris Extension Sets with microbore tubing Model 20022 and 30914 Is used to administer fluid and medications from a syringe to the patient through a needle or catheter inserted into the patient's artery or vein. These model codes are extension sets that can be used with IV administration sets. The set s components are commonly found on intravascular administration sets and extension sets. It includes a microbore tubing, a slide clamp, male and female luer.
Manufacturer(s)
CareFusion 303, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →