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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 8 of 8 Results
Related Medical Device Recalls
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Product Description
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Class
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Z-2723-2020 - Alaris Auto ID Module Model 8600, a modular infusion pump and monitoring system 1 08/06/2020 CareFusion 303, Inc.
Z-2721-2020 - Alaris EtCO2 Module Model 8300, a modular infusion pump and monitoring system 1 08/06/2020 CareFusion 303, Inc.
Z-2720-2020 - Alaris PCA Module Model 8120, a modular infusion pump and monitoring system 1 08/06/2020 CareFusion 303, Inc.
Z-2718-2020 - Alaris Pump Module Model 8100, a modular infusion pump and monitoring system 1 08/06/2020 CareFusion 303, Inc.
Z-2722-2020 - Alaris SpO2 Module Model 8210 and Model 8220, a modular infusion pump and monitoring system 1 08/06/2020 CareFusion 303, Inc.
Z-2719-2020 - Alaris Syringe Module Model 8110, a modular infusion pump and monitoring system 1 08/06/2020 CareFusion 303, Inc.
Z-2716-2020 - Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system 1 08/06/2020 CareFusion 303, Inc.
Z-2717-2020 - Alaris System PC Unit Model 8015, a modular infusion pump and monitoring system 1 08/06/2020 CareFusion 303, Inc.
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