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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-2822-2020 - Alaris Pump Module Model 8100 - Product Usage: is intended to provide trained healthcare caregivers a way to automate the programming of infusion parameters, thereby decreasing the amount of manual st... 2 08/19/2020 CareFusion 303, Inc.
Z-2823-2020 - Alaris Syringe Module Model 8110 - Product Usage: is intended to provide trained healthcare caregivers a way to automate the programming of infusion parameters, thereby decreasing the amount of manual... 2 08/19/2020 CareFusion 303, Inc.
Z-2826-2020 - Alaris SpO2 Module Model 8210 and Model 8220 - Product Usage: is intended to provide trained healthcare caregivers a way to automate the programming of infusion parameters, thereby decreasing the amou... 2 08/19/2020 CareFusion 303, Inc.
Z-2825-2020 - Alaris EtCO2 Module Model 8300 - Product Usage: is intended to provide trained healthcare caregivers a way to automate the programming of infusion parameters, thereby decreasing the amount of manual s... 2 08/19/2020 CareFusion 303, Inc.
Z-2824-2020 - Alaris PCA Module Model 8120 - Product Usage: is intended to provide trained healthcare caregivers a way to automate the programming of infusion parameters, thereby decreasing the amount of manual ste... 2 08/19/2020 CareFusion 303, Inc.
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