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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Diagnostic Equipment

BD Pyxis MedBank Dispensing Cabinets Recalled for Software Bug

Agency Publication Date: April 18, 2025
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Summary

CareFusion 303, Inc. is recalling 7,357 BD Pyxis MedBank Automated Dispensing Cabinets due to a software error that occurs during the restocking process. This bug causes bin inventory quantities to double, leading to inaccurate records and potential shortages. The recall includes various MedBank configurations such as MedPass, Mini, Tower, and MedFlex modules running software versions 2.4 and 1.2.3.23.

Risk

Inaccurate inventory counts can lead to delays in medical staff accessing essential medications or supplies during patient care. This delay could result in temporary impairment of bodily functions, though no injuries or deaths have been reported to date.

What You Should Do

  1. This recall involves various models of the BD Pyxis MedBank Automated Dispensing Cabinets, including MedPass, Mini, Tower, and MedFlex modules, specifically those running software versions 2.4 and 1.2.3.23.
  2. To determine if your facility is using an affected unit, identify the model name (REF) and software version located on the device label or system information screen. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.
  4. Contact CareFusion 303, Inc. directly for further instructions regarding a software update to resolve this issue.
  5. Call the FDA at 1-888-INFO-FDA (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 MedBank Automated Dispensing Cabinets
Variants: MedPass Module, Mini 1FH-1FM, Mini 1HH-1FH-1HM, Mini 1HH-1HM-1FM, Mini 2FH, Mini 2FM, Mini 2HH-1FH, Mini 2HH-1FM, Mini 3HH-1FG, Mini 3HH-1HM, Mini 4HH, Mini 4HM, Tower MN 10HH-1FH-1FM, Tower MN 10HH-2FH, Tower MN 10HH-2FM, Tower MN 12HH-1FF, Tower MN 12HH-1FH, Tower MN 12HH-1FM, Tower MN 14HH, Tower MN 1HH-1HM-2FM-4FF, Tower MN 2FH-2HM-4FM, Tower MN 2HH-10HM-1FM, Tower MN 2HH-1FH-5FM, Tower MN 2HH-2FH-4FM, Tower MN 2HH-4FH-2FM, Tower MN 2HH-4HM-4FM, Tower MN 2HH-6FM, Tower MN 2HH-6HM-3FM, Tower MN 2HH-8HM-2FM, Tower MN 2HM-6FM, Tower MN 3FH-4FM, Tower MN 3FH-8HH MedPass, Tower MN 3HH-7HM-2FM, Tower MN 4HH-10HM, Tower MN 4HH-1FH-2HM-3FM, Tower MN 4HH-1FH-4FM, Tower MN 4HH-1FH-4HM-2FM, Tower MN 4HH-2FH-2HM-2FM, Tower MN 4HH-2FH-3FM, Tower MN 4HH-3FH-2FM, Tower MN 4HH-4FH-1FM, Tower MN 4HH-4HM-3FM, Tower MN 4HH-5FH, Tower MN 4HH-5FM, Tower MN 4HH-6HM-2FM, Tower MN 4HM-5FM, Tower MN 5HH-3HM-3FM, Tower MN 5HH-9HM, Tower MN 6FH-1FM, Tower MN 6HH-1FH-2HM-2FM, Tower MN 6HH-1FH-3FM, Tower MN 6HH-2FH-2FM, Tower MN 6HH-4FH, Tower MN 6HH-4FM, Tower MN 6HH-4HM-2FM, Tower MN 6HH-8HM, Tower MN 7FH, Tower MN 7FM, Tower MN 7HH-1HM-3FM, Tower MN 8HH-1FH-2FM, Tower MN 8HH-2FH-1FM, Tower MN 8HH-2HM-2FM, Tower MN 8HH-3FF, Tower MN 8HH-3FH, Tower MN 8HH-3FM, MedFlex MN 1000 12HH, MedFlex MN 1000 2HH-2FM, MedFlex MN 1000 2HH-5FM, MedFlex MN 1000 4HH-4FM, MedFlex MN 1000 6HH-3FM, MedFlex MN 1000 8HH-2FM, MedFlex MN 2000 8HH-2FH, MedFlex MN 2000 8HH-2FM, MedBank Main, MedBank Mini Main, MedBank Tower Main, MedFlex, MedFlex 2.0
Model / REF (108):
139088-01
169-137
169-101
169-102
138902-01
169-104
169-105
169-106
138908-01
169-107
138906-01
169-108
169-110
139091-01
169-111
138910-01
169-112
169-113
138915-01
169-23
169-24
138955-01
169-25
138924-01
169-26
138960-01
169-27
138961-01
169-28
138926-01
138927-01
169-29
169-30
169-31
169-32
169-33
169-34
169-139
139125-01
169-38
138919-01
169-39
169-40
169-41
169-42
138933-01
169-140
169-43
169-44
138959-01
UDI:
10885403512544
10885403512568
10885403517181
10885403517167
10885403512704
GTIN:
10885403512544
10885403512568
10885403517181
10885403517167
10885403512704

Affects units running software versions 2.4 and 1.2.3.23.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96564
Status: Active
Manufacturer: CareFusion 303, Inc.
Sold By: Authorized Medical Distributors; Direct Sales to Hospitals; Healthcare Facilities
Manufactured In: United States
Units Affected: 7,357
Distributed To: Missouri, Michigan, Florida, Pennsylvania, South Carolina, Oregon, Arizona, Colorado, North Dakota, Georgia, Nebraska, Texas, Illinois, Ohio, Vermont, Indiana, Tennessee, Kentucky, Iowa, Montana, New York, California, Utah, Oklahoma, South Dakota, Washington, Alaska, Maine, Nevada, New Mexico, North Carolina, West Virginia, Louisiana, Minnesota, Idaho, Alabama, Virginia, Wisconsin, New Hampshire, Kansas, Massachusetts, Connecticut, Rhode Island, New Jersey, Maryland, Mississippi, Wyoming, District of Columbia, Delaware, Hawaii, Arkansas

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.