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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 30 of 34 Results
510(K) Number: K133532
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Alaris EtCO2 Module Model 8300, a modular infusion pump and monitoring system 1 08/06/2020 CareFusion 303, Inc.
Alaris PCA Module Model 8120, a modular infusion pump and monitoring system 1 08/06/2020 CareFusion 303, Inc.
Alaris Syringe Module Model 8110, a modular infusion pump and monitoring system 1 08/06/2020 CareFusion 303, Inc.
Alaris System PC Unit Model 8015. modular infusion pump and monitoring system 1 08/06/2020 CareFusion 303, Inc.
Alaris Pump Module Model 8100 1 08/06/2020 CareFusion 303, Inc.
Alaris System PC Unit Model 8000 modular infusion pump and monitoring system 1 08/06/2020 CareFusion 303, Inc.
CareFusion Alaris System, Alaris PC unit models 8000 and 8015 (UDI: 10885403801518) 1 03/05/2020 CareFusion 303, Inc.
Alaris Pump, Model 8100, with bezel mechanical assemblies manufactured with FR-110 plastic resin. ... 1 07/16/2019 CareFusion 303, Inc.
Alaris Pump Module, Model 8100, serviced/repaired by Infusion Pump Repair with an impacted bezel rep... 1 05/10/2021 Infusion Pump Repair
Aftermarket Alaris Infusion Pump Module Model 8100 Front Bezel, installed by Pacific Medical Group (... 1 04/19/2021 Pacific Medical Group Inc.
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