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CareFusion 303, Inc. recalls VersaSafe Extension Set, Model No. 21000M-007
Recalled December 11, 2013 · FDA recall Z-0435-2014 · CareFusion 303
Hazard
CareFusion is recalling the VersaSafe Extension Intravascular Administration Set because it may have excessive adhesive which will prevent the male spin collar to operate as intended. · FDA Class II
Units
3500 units
Sold at
Nationwide Distribution.
Description
CareFusion is recalling the VersaSafe Extension Intravascular Administration Set because it may have excessive adhesive which will prevent the male spin collar to operate as intended.
Product
VersaSafe Extension Set, Model No. 21000M-007
Manufacturer(s)
CareFusion 303, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →