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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 29 Results
Product: alaris Class 1 Recall Date from: 01/01/2020
 
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CareFusion Alaris Pump Module, Model 8100 1 03/05/2020 CareFusion 303, Inc.
CareFusion Alaris System, Alaris PC unit models 8000 and 8015 (UDI: 10885403801518) 1 03/05/2020 CareFusion 303, Inc.
CareFusion Alaris PCA Module, Model 8120 1 03/05/2020 CareFusion 303, Inc.
CareFusion Alaris Syringe Module, Model 8110 1 03/05/2020 CareFusion 303, Inc.
Alaris Pump Module Model 8100 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 System PC Unit Model 8000 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 8000, 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.
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