CareFusion 303, Inc.: 86 recalls on record

Recalls filed with 1 agency: FDA (86).

First recall on record: August 1, 2012. Most recent: June 10, 2026.

Risk classification: Class I: 16 · Class II: 70

Most recent recalls

DateAgencyProduct
September 11, 2024FDABKIT BD Pyxis QFill Replenishment Station, REF: 155197-01, medication cabinet systemZ-2948-2024
August 14, 2024FDABD PYXIS MEDBANK TWR MN CR-14HH-P, REF: 169-86 containing software version 3.9.1.9Z-2492-2024
August 14, 2024FDABD PYXIS MEDBANK TWR MN CR-10HH-2FH-P, REF: 169-82 containing software version 3.9.1.9Z-2488-2024
August 14, 2024FDABD PYXIS MEDBANK TWR MN CR-8HH-3FM-P, REF: 169-99 containing software version 3.9.1.9Z-2503-2024
August 14, 2024FDABD PYXIS MEDBANK TWR MN CR-2HH-6FH, REF: 169-88 containing software version 3.9.1.9Z-2493-2024
August 14, 2024FDABD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P, REF: 169-96 containing software version 3.9.1.9Z-2500-2024
August 14, 2024FDABD PYXIS MEDBANK TWR MN CR-2HH-6FM, REF: 169-89 containing software version 3.9.1.9Z-2494-2024
August 14, 2024FDABD PYXIS MEDBANK MINI CR-4HH-P, REF: 169-115 containing software version 3.9.1.9Z-2486-2024
August 14, 2024FDABD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P, REF: 169-97 containing software version 3.9.1.9Z-2501-2024
August 14, 2024FDABD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P, REF: 169-92 containing software version 3.9.1.9Z-2497-2024
August 14, 2024FDABD PYXIS MEDBANK TWR MN CR-12HH-1FH, REF: 169-84 containing software version 3.9.1.9Z-2490-2024
August 14, 2024FDABD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P, REF: 169-90 containing software version 3.9.1.9Z-2495-2024
August 14, 2024FDABD PYXIS MDBNK TWR MN CR-4HH-5FM-P RxNow, REF: 169-131 containing software version 3.9.1.9Z-2487-2024
August 14, 2024FDABD PYXIS MEDBANK TWR MN CR-4HH-5FM-P, REF: 169-91 containing software version 3.9.1.9Z-2496-2024
August 14, 2024FDABD PYXIS MEDBANK TWR MN CR-6HH-4FM-P, REF: 169-94 containing software version 3.9.1.9Z-2499-2024
August 14, 2024FDABD PYXIS MEDBANK MINI CR-2HH-1FH-P, REF: 169-114 containing software version 3.9.1.9Z-2485-2024
August 14, 2024FDABD PYXIS MEDBANK TWR MN CR-12HH-1FM-P, REF: 169-85 containing software version 3.9.1.9Z-2491-2024
August 14, 2024FDABD PYXIS MEDBANK TWR MN CR-6HH-2FH-2FM-P, REF: 169-93 containing software version 3.9.1.9Z-2498-2024
August 14, 2024FDABD PYXIS MEDBANK TWR MN CR-8HH-3FH-P, REF: 169-98 containing software version 3.9.1.9Z-2502-2024
August 14, 2024FDABD PYXIS MEDBANK TWR MN CR-10HH-2FM-P, REF: 169-83 containing software version 3.9.1.9Z-2489-2024
July 24, 2024FDABD Pyxis: MedStation ES (Main), REF: 323; MedStation ES Tower, REF: 352; Anesthesia Sta…Z-2374-2024
July 10, 2024FDABD Alaris System Manager REF: 9601, compatible with BD Alaris PC UnitsZ-2262-2024
July 10, 2024FDABD Pyxis, Name/REF: BD PYXIS MB TOWER MAIN/ 169-153, BD PYXIS MB TOWER MAIN CR/ 169-154,…Z-2256-2024
July 10, 2024FDABD Pyxis, Name/REF: MEDBANK MINI 1FH-1FM/ 169-137, MEDBANK MINI 1FH-2HH MEDPASS/ 169-1…Z-2255-2024
June 5, 2024FDABD Pyxis MedStation 4000 System, REF: 303, Medication CabinetZ-1928-2024

Questions about this company

How many recalls does CareFusion 303, Inc. have?
Recalert has 86 U.S. recalls on record for CareFusion 303, Inc., published between August 1, 2012 and June 10, 2026.
Which agencies have handled CareFusion 303, Inc. recalls?
CareFusion 303, Inc. appears as the recalling firm in recalls from: FDA (86).

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