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CareFusion 303, Inc. recalls MaxGuard Extension Set with Injection Site and 0.2 micron filter, Model No. ME3305
Recalled March 22, 2017 · FDA recall Z-1464-2017 · CareFusion 303
Hazard
CareFusion is recalling the MaxGuard Extension Set with Injection Site and 0.2 micron filter because of reports of separation and/or leakages between the Y-connector and tubing. · FDA Class II
Units
1,200 units
Sold at
US Distribution including MA and MD
Description
CareFusion is recalling the MaxGuard Extension Set with Injection Site and 0.2 micron filter because of reports of separation and/or leakages between the Y-connector and tubing.
Product
MaxGuard Extension Set with Injection Site and 0.2 micron filter, Model No. ME3305
Manufacturer(s)
CareFusion 303, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →