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U.S. Department of Health and Human Services

Medical Device Recalls
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31 to 34 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 EtCO2 Module Model 8300 - Product Usage: is intended to provide trained healthcare caregivers... 2 08/19/2020 CareFusion 303, Inc.
Alaris Auto ID Module Model 8600, a modular infusion pump and monitoring system 1 08/06/2020 CareFusion 303, Inc.
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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