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Medium RiskFDA Device
Medical Devices

BD Pyxis Automated Dispensing Cabinets Recalled for Software Bug

Agency Publication Date: April 9, 2025
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Summary

CareFusion 303, Inc. (BD) is recalling approximately 7,357 units of BD Pyxis automated dispensing cabinets, including MedBank Mini, MedBank Tower, MedFlex, and MedBank MedPass models, due to a software bug. This defect prevents the system from correctly calculating medication counts and can cause dispensing drawers to open more times than necessary during a transaction. The cabinets are used in clinical settings to securely store and dispense patient medications. No incidents or injuries have been reported to date.

Risk

The software bug can cause incorrect medication quantities to be recorded and allow dispensing drawers to open multiple times, which may result in a patient receiving more than their intended dose of medication.

What You Should Do

  1. This recall affects BD Pyxis MedBank Mini, BD Pyxis MedBank Tower, BD Pyxis MedFlex, and BD Pyxis MedBank MedPass automated dispensing cabinets with software versions 1.2.3.23 or 2.4.
  2. Check the model number (REF), GTIN, and software version on the dispensing cabinet identification label to determine if your unit is affected. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled device immediately. Contact CareFusion 303, Inc. or your equipment distributor to arrange for a software correction or to coordinate a return or replacement.
  4. Call the FDA Consumer Complaint hotline at 1-888-463-6332 or visit www.fda.gov/medical-devices/medical-device-recalls for additional information.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: BD Pyxis Automated Dispensing Cabinets (ADC)
Variants: Software Version 1.2.3.23, Software Version 2.4, MedBank Mini, MedBank Tower, MedFlex, MedPass
Model / REF (267):
169-143
169-145
169-144
169-142
139088-01
155288-01
169-137
155311-01
169-151
138921-01
155159-01
169-101
139122-01
155160-01
169-102
138912-01
155161-01
169-103
138902-01
169-104
138903-01
155163-01
169-105
138908-01
169-106
138906-01
155165-01
169-107
169-152
138907-01
155166-01
169-108
139131-01
155167-01
169-109
139091-01
155168-01
169-110
138909-01
155169-01
169-111
138910-01
155310-01
169-112
169-150
138915-01
155171-01
169-113
138943-01
155081-01
GTIN (84):
10885403512568
10885403508721
10885403512544
10885403510847
10885403504655
10885403504662
10885403504679
10885403504686
10885403504693
10885403504570
10885403504587
10885403504594
10885403504600
10885403510830
10885403504617
10885403503870
10885403503887
10885403503894
10885403503900
10885403503917
10885403503726
10885403503733
10885403509926
10885403510779
10885403503740
10885403510793
10885403503757
10885403510786
10885403503764
10885403503771
10885403503788
10885403503795
10885403509933
10885403503801
10885403503818
10885403503696
10885403504198
10885403503702
10885403504204
10885403504211
10885403510526
10885403504228
10885403510762
10885403504235
10885403504242
10885403504259
10885403503719
10885403504266
10885403504273
10885403504280

Affected units are clinical automated dispensing cabinets (ADC) with software version 1.2.3.23 or 2.4.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96557
Status: Active
Manufacturer: CareFusion 303, Inc.
Sold By: Clinical settings; Healthcare facilities
Manufactured In: United States
Units Affected: 7357
Distributed To: California, Texas, Wisconsin, Colorado, Alaska, Virginia, Tennessee, Washington, North Carolina, New York, Mississippi, Florida, Kansas, Michigan, Indiana, Minnesota, Montana, Kentucky, Missouri, Utah, New Jersey, Ohio, Pennsylvania, North Dakota, Oregon, Nebraska, South Dakota, Nevada, Oklahoma, Georgia, Massachusetts, Iowa, Hawaii, Maine, Arizona, Illinois, South Carolina, Louisiana, West Virginia, Alabama, Idaho, New Mexico, District of Columbia, New Hampshire, Vermont, Connecticut, Maryland, Arkansas, Wyoming

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.