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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 30 Results
Product: alaris Class 1 Recall Date from: 01/01/2020
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Product Description
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FDA Recall
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Alaris Auto ID Module Model 8600, a modular infusion pump and monitoring system 1 08/06/2020 CareFusion 303, Inc.
Alaris SpO2 Module Model 8210 and Model 8220, a modular infusion pump and monitoring system 1 08/06/2020 CareFusion 303, Inc.
Alaris EtCO2 Module Model 8300, a modular infusion pump and monitoring system 1 08/06/2020 CareFusion 303, Inc.
Alaris Pump Module Model 8100, a modular infusion pump and monitoring system 1 08/06/2020 CareFusion 303, Inc.
Alaris System PC Unit Model 8015, a modular infusion pump and monitoring system 1 08/06/2020 CareFusion 303, Inc.
BD Alaris System; Alaris Syringe Module Model 8110; BD Alaris System; Alaris PCA Module Model 8120... 1 09/04/2020 CareFusion 303, Inc.
Alaris System PC Unit Model 8015 1 09/04/2020 CareFusion 303, Inc.
BD Alaris System PC Unit Model 8100 (Pump Module) and Pump Module Door Assembly Replacement Kits (P/... 1 09/12/2020 CareFusion 303, Inc.
BD Alaris Infusion Pump Module Model 8100 Pump Module Keypad; and Pump Module Door Assembly Replacem... 1 04/01/2021 CareFusion 303, Inc.
Alaris Infusion Pump Module, Model 8100, serviced/repaired by Tenacor with an impacted bezel repair ... 1 04/02/2021 Tenacore LLC
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