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CareFusion 303 Recalls
173 recalls on record · August 1, 2012 to June 10, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
September 11, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BKIT BD Pyxis QFill Replenishment Station, REF: 155197-01, medication cabinet system
Hazard: Due to software issue, there is a potential when a restock label is printed for a medication stored in a non-CUBIE location, that the incorrect bin for the medication is printed on the label.
September 11, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis QFill Replenishment Station, REF: 138904-01, medication cabinet system
Hazard: Due to software issue, there is a potential when a restock label is printed for a medication stored in a non-CUBIE location, that the incorrect bin for the medication is printed on the label.
August 14, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P, REF: 169-99 containing software version 3.9.1.9
Hazard: Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
August 14, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P, REF: 169-98 containing software version 3.9.1.9
Hazard: Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
August 14, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P, REF: 169-97 containing software version 3.9.1.9
Hazard: Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
August 14, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P, REF: 169-96 containing software version 3.9.1.9
Hazard: Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
August 14, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P, REF: 169-94 containing software version 3.9.1.9
Hazard: Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
August 14, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD PYXIS MEDBANK TWR MN CR-6HH-2FH-2FM-P, REF: 169-93 containing software version 3.9.1.9
Hazard: Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
August 14, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P, REF: 169-92 containing software version 3.9.1.9
Hazard: Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
August 14, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P, REF: 169-91 containing software version 3.9.1.9
Hazard: Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
August 14, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P, REF: 169-90 containing software version 3.9.1.9
Hazard: Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
August 14, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD PYXIS MEDBANK TWR MN CR-2HH-6FM, REF: 169-89 containing software version 3.9.1.9
Hazard: Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
August 14, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD PYXIS MEDBANK TWR MN CR-2HH-6FH, REF: 169-88 containing software version 3.9.1.9
Hazard: Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
August 14, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD PYXIS MEDBANK TWR MN CR-14HH-P, REF: 169-86 containing software version 3.9.1.9
Hazard: Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
August 14, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P, REF: 169-85 containing software version 3.9.1.9
Hazard: Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
August 14, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD PYXIS MEDBANK TWR MN CR-12HH-1FH, REF: 169-84 containing software version 3.9.1.9
Hazard: Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
August 14, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P, REF: 169-83 containing software version 3.9.1.9
Hazard: Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
August 14, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P, REF: 169-82 containing software version 3.9.1.9
Hazard: Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
August 14, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD PYXIS MDBNK TWR MN CR-4HH-5FM-P RxNow, REF: 169-131 containing software version 3.9.1.9
Hazard: Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
August 14, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD PYXIS MEDBANK MINI CR-4HH-P, REF: 169-115 containing software version 3.9.1.9
Hazard: Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
August 14, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD PYXIS MEDBANK MINI CR-2HH-1FH-P, REF: 169-114 containing software version 3.9.1.9
Hazard: Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
July 24, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis: MedStation ES (Main), REF: 323; MedStation ES Tower, REF: 352; Anesthesia Station ES, REF: 327; CII Safe ES
Hazard: If automated dispensing cabinets have specific software versions, and Component Manager was configured to "installed mode", and software patch KB 5033688 was installed in the production environment, then this will will lead to an error that prevents the user from accessing the dispensing software application, which may delay accessing medication.
July 10, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD Alaris System Manager REF: 9601, compatible with BD Alaris PC Units
Hazard: Due to a software issue the PC unit may not connect to the server which could impact wireless data transmission to and from the server.
July 10, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis, Name/REF: BD PYXIS MB TOWER MAIN/ 169-153, BD PYXIS MB TOWER MAIN CR/ 169-154, BD PYXIS MB TOWER MAIN W/MP/ 1
Hazard: Multiple socket-outlet power strips that shipped with automated dispensing cabinet devices have not been certified to International Electrotechnical Commission (IEC) electrical standards when used as a system with automated dispensing cabinet devices, so use may expose user to leakage currents that could cause varying degrees of harm from a minor shock to permanent impairment.
July 10, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis, Name/REF: MEDBANK MINI 1FH-1FM/ 169-137, MEDBANK MINI 1FH-2HH MEDPASS/ 169-151, MEDBANK MINI 1HH-1FH-1HM/
Hazard: Multiple socket-outlet power strips that shipped with automated dispensing cabinet devices have not been certified to International Electrotechnical Commission (IEC) electrical standards when used as a system with automated dispensing cabinet devices, so use may expose user to leakage currents that could cause varying degrees of harm from a minor shock to permanent impairment.
June 5, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis(TM) Anesthesia Station 4000, REF: 338
Hazard: Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
June 5, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis" Anesthesia Station ES, REF: 327
Hazard: Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
June 5, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis MedStation 4000 7-Drawer Auxiliary Tower, REF: 306
Hazard: Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
June 5, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis" MedStation ES 7-Drawer Auxiliary Tower, REF: 324
Hazard: Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
June 5, 2024Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis MedStation 4000 System, REF: 303, Medication Cabinet
Hazard: Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.