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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 34 Results
510(K) Number: K133532
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Product Description
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FDA Recall
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Alaris EtCO2 Module Model 8300 - 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.
Alaris PCA Module Model 8120 - Product Usage: is intended to provide trained healthcare caregivers a... 2 08/19/2020 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 Pump Module Model 8100 - Product Usage: is intended to provide trained healthcare caregivers ... 2 08/19/2020 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.
Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system 1 08/06/2020 CareFusion 303, Inc.
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.
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