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CareFusion 303, Inc. recalls MaxGuard Extension Set, Model No. ME2064, MP9009C, MP9209, MP9254C The MaxGuard extension sets are used to administer f
Recalled March 22, 2017 · FDA recall Z-1482-2017 · CareFusion 303
Hazard
CareFusion is recalling the MaxGuard Extension Set due to reports of leaks occurring with the 0.2 micron filter. · FDA Class II
Units
12,850 units
Sold at
Nationwide Distribution
Description
CareFusion is recalling the MaxGuard Extension Set due to reports of leaks occurring with the 0.2 micron filter.
Product
MaxGuard Extension Set, Model No. ME2064, MP9009C, MP9209, MP9254C The MaxGuard extension sets are used to administer fluids from a container to a patient s vascular system through a needle or catheter inserted into the patient s artery or vein. The extension sets may incorporate components that aid in the prevention of accidental needle sticks. The set s components are commonly found on intravascular administration sets and extension sets
Manufacturer(s)
CareFusion 303, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →