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CareFusion 303, Inc. recalls Alaris System PC Unit Model 8000 modular infusion pump and monitoring system
Recalled August 12, 2020 · FDA recall Z-2740-2020 · CareFusion 303
Hazard
If one or more screws or washers are loose or missing causing the battery not to be properly secured to the PC Unit, that is running on battery power, the system may experience a power loss with a prolonged, non-silenceable alarm. Power loss may result in an interruption of patient therapy or monitoring. · FDA Class I
Units
37141
Sold at
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Description
If one or more screws or washers are loose or missing causing the battery not to be properly secured to the PC Unit, that is running on battery power, the system may experience a power loss with a prolonged, non-silenceable alarm. Power loss may result in an interruption of patient therapy or monitoring.
Product
Alaris System PC Unit Model 8000 modular infusion pump and monitoring system
Manufacturer(s)
CareFusion 303, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →