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CareFusion 303, Inc. recalls Alaris Pump Module model 8100
Recalled July 19, 2017 · FDA recall Z-2700-2017 · CareFusion 303
Hazard
There is a potential risk that could cause unintended flow in the older, centered sear door latch design in the Alaris Pump module model 8100. · FDA Class II
Units
35,940 units
Sold at
US and Canada
Description
There is a potential risk that could cause unintended flow in the older, centered sear door latch design in the Alaris Pump module model 8100.
Product
Alaris Pump Module model 8100
Manufacturer(s)
CareFusion 303, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →