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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
510(K) Number: K133532
 
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BD Alaris System. The EtCO2 module is a capnograph indicated for continuous, noninvasive monitoring ... 2 09/03/2020 CareFusion 303, Inc.
Alaris Syringe Module Model 8110 - Product Usage: is intended to provide trained healthcare caregive... 2 08/19/2020 CareFusion 303, Inc.
Alaris PCA Module Model 8120 - Product Usage: is intended to provide trained healthcare caregivers a... 2 08/19/2020 CareFusion 303, Inc.
Alaris EtCO2 Module Model 8300 - Product Usage: is intended to provide trained healthcare caregivers... 2 08/19/2020 CareFusion 303, Inc.
Alaris Pump Module Model 8100 - Product Usage: is intended to provide trained healthcare caregivers ... 2 08/19/2020 CareFusion 303, Inc.
Alaris SpO2 Module Model 8210 and Model 8220 - Product Usage: is intended to provide trained healthc... 2 08/19/2020 CareFusion 303, Inc.
BD Alaris PCU REF 8015 1 11/07/2023 CareFusion 303, Inc.
BD Alaris Syringe Module, REF 8110 1 11/07/2023 CareFusion 303, Inc.
Alaris PCA Module 8120 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)
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