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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 34 Results
Product: alaris Class 1 Recall Date from: 01/01/2020
 
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BD Alaris infusion Pump Module 8100, REF: 8100; KIT, BEZEL ASSY 8100BD, REF: 49000437; KIT ASSY O... 1 11/20/2025 CareFusion 303, Inc.
BD Alaris Pump Infusion Sets for the following reference numbers: C24101E, Amber Tubing, 15 Micron... 1 10/08/2025 CareFusion 303, Inc.
BD Alaris Pump Infusion Sets REF: 10013186, BD Alaris Pump Infusion Set, Back Check Valve, 3 Smar... 1 08/06/2025 CareFusion 303, Inc.
BD Alaris Pump Module Model, 8100 with Guardrails, Suite MX software versions 1 08/06/2025 CareFusion 303, Inc.
BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software 1 03/13/2025 CareFusion 303, Inc.
Alaris PCA Module 8120 1 11/07/2023 CareFusion 303, Inc.
BD Alaris Syringe Module, REF 8110 1 11/07/2023 CareFusion 303, Inc.
BD Alaris PCU REF 8015 1 11/07/2023 CareFusion 303, Inc.
Alaris Infusion Pump Module, Model 8100, serviced/repaired by Biomedical Equipment Service Co. (BMES... 1 08/06/2021 BioMedical Equipment Service Co (BMES)
Alaris Infusion Pump Module, Model 8100, serviced/repaired by The Biomed Guys, with the impacted bez... 1 06/01/2021 The Biomed Guys
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