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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 19 Results
Related Medical Device Recalls
 
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Product Description
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Z-2503-2024 - BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P, REF: 169-99 containing software version 3.9.1.9 2 08/02/2024 FEI # 2016493
CareFusion 303, Inc.
Z-2502-2024 - BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P, REF: 169-98 containing software version 3.9.1.9 2 08/02/2024 FEI # 2016493
CareFusion 303, Inc.
Z-2501-2024 - BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P, REF: 169-97 containing software version 3.9.1.9 2 08/02/2024 FEI # 2016493
CareFusion 303, Inc.
Z-2500-2024 - BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P, REF: 169-96 containing software version 3.9.1.9 2 08/02/2024 FEI # 2016493
CareFusion 303, Inc.
Z-2499-2024 - BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P, REF: 169-94 containing software version 3.9.1.9 2 08/02/2024 FEI # 2016493
CareFusion 303, Inc.
Z-2498-2024 - BD PYXIS MEDBANK TWR MN CR-6HH-2FH-2FM-P, REF: 169-93 containing software version 3.9.1.9 2 08/02/2024 FEI # 2016493
CareFusion 303, Inc.
Z-2497-2024 - BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P, REF: 169-92 containing software version 3.9.1.9 2 08/02/2024 FEI # 2016493
CareFusion 303, Inc.
Z-2496-2024 - BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P, REF: 169-91 containing software version 3.9.1.9 2 08/02/2024 FEI # 2016493
CareFusion 303, Inc.
Z-2495-2024 - BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P, REF: 169-90 containing software version 3.9.1.9 2 08/02/2024 FEI # 2016493
CareFusion 303, Inc.
Z-2494-2024 - BD PYXIS MEDBANK TWR MN CR-2HH-6FM, REF: 169-89 containing software version 3.9.1.9 2 08/02/2024 FEI # 2016493
CareFusion 303, Inc.
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