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CareFusion 303, Inc. recalls SmartSite Extension Set, Model No. 20029E. Used to administer fluid and medications through a needle or catheter inserte
Recalled November 11, 2015 · FDA recall Z-0221-2016 · CareFusion 303
Hazard
CareFusion is recalling the SmartSite Extension Set due to disconnection and leakage issues. · FDA Class II
Units
21,000 units
Sold at
Distributed US (nationwide) and in Canada.
Description
CareFusion is recalling the SmartSite Extension Set due to disconnection and leakage issues.
Product
SmartSite Extension Set, Model No. 20029E. 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 →