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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.

June 10, 2026Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet
Hazard: Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
June 10, 2026Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet
Hazard: Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
June 10, 2026Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis MedStation ES Tower REF: 352 Medication cabinet
Hazard: Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
June 10, 2026Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis Mini Main REF: 349 Medication cabinet
Hazard: Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
June 10, 2026Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet
Hazard: Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
June 10, 2026Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet
Hazard: Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
June 10, 2026Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis MedStation ES REF: 323 Medication cabinet
Hazard: Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
June 10, 2026Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis MedStation 4000 REF: 303 Medication cabinet
Hazard: Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
April 1, 2026Medical DevicesFDA
CareFusion 303, Inc. recalls BD Alaris" System with Guardrails" Suite MX with Point of Care Unit
Hazard: Due to product labeling not indicating which Transport Layer Security (TLS) version that must be enabled on hospital network to ensure secure Wi-Fi communication with Point-of-Care Units
February 4, 2026Medical DevicesFDA
CareFusion 303, Inc. recalls BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 The BD AlarisTM System with Guardrails" Suite MX is a
Hazard: Due to a number of modules flashed with a date and time associated with the daylight savings time (DST) adjustment that may cause connectivity issue with hospital networks. This issue only affects the Interoperability workflow for devices with a DST invalid timestamp, impacting connectivity of the PCU to the hospital network
January 14, 2026Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis ES Enterprise Server Catalog Numbers 1115-00, 137672-02,137672-03 137671-02, 137671-03, 137670-02, 137670-03,
Hazard: Due a software issue that may result in equipment not receiving timely updates of patient, medication, or related information from enterprise systems.
December 31, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis MedStation ES, REF: 323, BD Pyxis MedStation ES 7 Drawer Auxiliary, REF: 324, BD Pyxis MedStation ES Tower
Hazard: Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer firmware update, which caused a Cubie Insert event which prompts software to generate a duplicate address, which causes an error and the drawer to fail, which may lead to inability or delay in accessing stored items, delay in the replenishment of ADCs or patient specific medications stored outside of ADCs.
November 26, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls BD Alaris infusion Pump Module 8100, REF: 8100; KIT, BEZEL ASSY 8100BD, REF: 49000437; KIT ASSY ONE PIECE BEZEL 8100,
Hazard: If infusion pump is dropped or severely jarred this may damage the pump module bezel assembly, which can cause under-infusion, over-infusion, unregulated flow, or pump module failure to calibrate; so dropped/jarred pumps should be removed from use, tested, and inspected by qualified service personnel prior to reuse; tip sheet, cleaning and disinfecting procedure and reference guide updated.
November 5, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls All Serial Numbers/BD Pyxis CII Safe ES Tower Main, REF: 1116-00
Hazard: Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
November 5, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis Pro MedStation Main, REF: 1155-00
Hazard: Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
November 5, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls Various models of BD Pyxis Pro 7-Drawer Auxiliary, Reference numbers: 1149-00 and 1152-00
Hazard: Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
November 5, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls Various models of BD Pyxis MedFlex, Reference numbers: 1119-00 1139-00 139038-01 139039-01 139040-01 139041-01 13
Hazard: Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
November 5, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls Various models of BD Pyxis Medbank: Reference numbers: 1137-00 1145-00 1146-00 1147-00 1148-00 138902-01 138903-
Hazard: Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
October 15, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls BD Alaris Pump Infusion Sets for the following reference numbers: C24101E, Amber Tubing, 15 Micron Filter, 0.2 Micron
Hazard: Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time to alarm, and post-occlusion bolos volume.
September 3, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis Product Name / UDI-DI code / Catalog No. BD Pyxis" MedStation" 4000 Main / 10885403512629 / 303 BD Pyxis"
Hazard: Antivirus software was not consistently installed on impacted devices during the implementation process.
August 20, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls Description/REF: BD PYXIS MEDBANK MINI 1FH-1FM/169-137, BD PYXIS MEDBANK MINI 4HM/169-113, BD PYXIS MEDBANK MINI 4HH
Hazard: Reports of delayed access to medication in automated dispensing cabinets because of the override/Add Item workflow.
August 13, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls BD Alaris Pump Infusion Sets REF: 10013186, BD Alaris Pump Infusion Set, Back Check Valve, 3 SmartSite Y-sites LVP 60
Hazard: Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time to alarm, and post-occlusion bolos volume.
August 13, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls BD Alaris Pump Module Model, 8100 with Guardrails, Suite MX software versions
Hazard: Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time to alarm, and post-occlusion bolos volume.
July 2, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls Product Name [REF]: Supply Server, CCE Enterprise SW Site License (2-5), BD Pyxis Logistics [806], BD Pyxis MedStation 4
Hazard: During automated dispensing cabinet upgrade/installation/reimaging, component manager was left in installed mode, and if a Microsoft patch is then installed this may lead to an error preventing user access to the dispensing software application, which may lead to delay in access to medications/supplies, and delivery/replenishment of patient specific orders; which may lead to delay in patient care.
April 30, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls BD PYXIS MEDBANK (Name, REF): MEDPASS MODULE, 139088-01; MINI 1FH-1FM, 169-137; MINI 1HH-1FH-1HM, 169-101; MINI 1HH-
Hazard: Users trying to restock a single bin location of an automated dispensing cabinet, during pocket exchange restocking workflow, may experience a software issue that results in 2 destock transactions and 2 stock transactions, which results in doubling the bin quantity, which may result in a delay in access to desired medications and/or supplies, which may lead to temporary body function impairment.
April 23, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls MEDFLEX, REF: 1119-00; MEDBANK MAIN, REF: 1137-00; MEDFLEX 2.0, REF: 1139-00; MEDBANK TOWER MAIN, REF: 1145-00; MEDBANK
Hazard: If "Clear All" selected medications is selected on patient profile, the automated dispensing cabinet may allow dispensing of medication without first requiring the RxVerify Validation Code be entered/without validation from a pharmacist, which could lead to unintended and incorrect medication removal.
April 16, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis MedBank CUBIE Replenishment Station Product / Material ID BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P / 155141-01
Hazard: Due to a software issue, when attempting to restock the automated dispensing cabinet, user have received the banner message "Stocking window has passed, or item has been removed from purchase order. Please contact Pharmacy for assistance". When this occurs, the medication cannot be restocked and can potentially lead to delays in accessing medication for patients.
April 16, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower, BD Pyxis" MedFlex, BD Pyxis" MedBank" MedPass are automated dispen
Hazard: Due to a software bug, automated dispensing cabinet is unable to calculate countback discrepancies during the issue process, which causes incorrect transaction quantity to be recorded. This bug can also result in the CUBIE opening more times than needed for the transaction to be completed, which may result in a patient receiving more than the intended dose of medication.
March 26, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis: Anesthesia Station ES, REF: 327, MedStation ES, REF: 323, MedStation ES Tower, REF: 352, CII Safe ES, REF
Hazard: Sync timeout may occur between the server and automated dispensing device, due to a server software error which may occur if syncing a large amount of data that takes excessive time, which may cause the dispensing devices to become disconnected from the ES server; dispensing devices will not receive updated information, which may lead to incorrect therapy, and delay in accessing medication.
March 19, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls BD Care Coordination Engine (CCE) Infusion Adapter, Safety Management Software
Hazard: Software issue that may result in outdated automated programming request(APR) being sent to the progressive care unit (PCU).
CareFusion 303 Recalls | RecallWatchUSA