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CareFusion 303, Inc. recalls Alaris PC units, Model No. 8015. Infusion pump.
Recalled April 1, 2015 · FDA recall Z-1311-2015 · CareFusion 303
Hazard
CareFusion is recalling the Alaris PC unit because of an error code. The error code may occur upon power on during the "Power-On Self Test" due to a keypad issue. · FDA Class II
Units
56,015 units
Sold at
Worldwide Distribution - USA (nationwide), Canada, European Union, Singapore and Australia.
Description
CareFusion is recalling the Alaris PC unit because of an error code. The error code may occur upon power on during the "Power-On Self Test" due to a keypad issue.
Product
Alaris PC units, Model No. 8015. Infusion pump.
Manufacturer(s)
CareFusion 303, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →