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CareFusion 303, Inc. recalls SmartSite Low Sorbing Infusion Set, Model No. 10015862 The SmartSite Infusion Sets are used to administer fluid and med

Recalled February 11, 2015 · FDA recall Z-1053-2015 · CareFusion 303

Hazard
CareFusion is recalling the SmartSite Low Sorbing Infusion set due to disconnection and leakage issues. · FDA Class II
Units
7,440 units
Sold at
Nationwide Distribution

Description

CareFusion is recalling the SmartSite Low Sorbing Infusion set due to disconnection and leakage issues.

Product
SmartSite Low Sorbing Infusion Set, Model No. 10015862 The SmartSite Infusion Sets are used to administer fluid and medications through a needle or catheter inserted into the patient's artery or vein. The set is comprised of components commonly found on intravascular administration sets and extension sets. It includes a SmartSite bag access port, a non-vented drip chamber, roller clamp, infusion pump segment, a male luer, and low sorbing tubing.
Manufacturer(s)
CareFusion 303, Inc.

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

CareFusion 303, Inc. recalls SmartSite Low Sorbing Infusion Set, Model No. 10015862 The SmartSite Infusion Sets are used to administer fluid and med | RecallWatchUSA