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CareFusion 303, Inc. recalls SmartSite Extension Set, Model No. 20029E, intravascular administration set.
Recalled April 23, 2014 · FDA recall Z-1459-2014 · CareFusion 303
Hazard
Disconnections and leakages at the connection of the smallbore tubing and the SmartSite Y-port. · FDA Class II
Units
7,700 units
Sold at
USA Nationwide Distribution in the states of: AR, AZ, CA, CO, FL, ID, MD, MI, NC, NV, OK, OR, PA, TX, VA, WI
Description
Disconnections and leakages at the connection of the smallbore tubing and the SmartSite Y-port.
Product
SmartSite Extension Set, Model No. 20029E, intravascular administration set.
Manufacturer(s)
CareFusion 303, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →