Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

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.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Device
Medical Devices

BD Pyxis MedBank Cabinets Recalled for Medication Dispensing Error

Agency Publication Date: April 11, 2025
Share:
Sign in to monitor this recall

Summary

CareFusion 303, Inc. is recalling 2,679 BD Pyxis MedBank automated dispensing cabinets and associated software. A software error can allow hospital staff to remove medications from the cabinet without a required pharmacist's validation code if the "Clear All" option is selected on a patient's profile. This defect affects several models including the MedFlex, MedBank Tower, and MedBank Mini systems running specific software versions.

Risk

The software error may lead to the unintended and incorrect removal of medications from the dispensing cabinets. This poses a risk of medication errors, where patients could receive the wrong drug or incorrect dosage, although no injuries have been reported to date.

What You Should Do

  1. This recall affects BD Pyxis MedBank automated dispensing cabinets (Main, Mini, and Tower models) and MedFlex systems running software versions 2.1.2.11, 2.2.1.8, 2.31.8, 2.3.2.1, or 2.4.2.26.
  2. Identify affected cabinets by checking the REF (catalog) number and UDI-DI code on the device label or within the software system configuration. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled device. Contact CareFusion 303, Inc. or your equipment distributor immediately to arrange for a software update, correction, or return of the affected system.
  4. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) if you have further questions regarding this medical device recall.

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 Cabinets and Software
Variants: Software version 2.1.2.11, Software version 2.2.1.8, Software version 2.31.8, Software version 2.3.2.1, Software version 2.4.2.26, MedFlex, MedFlex 2.0, MedBank Main, MedBank Tower Main, MedBank Mini Main
Model / REF (91):
1119-00
1137-00
1139-00
1145-00
1147-00
139090-01
169-100
169-101
169-102
169-103
169-104
169-105
169-106
169-107
169-108
169-109
169-110
169-111
169-112
169-113
169-132
169-137
169-138
169-139
169-153
169-155
169-156
169-159
169-160
169-161
169-162
169-23
169-24
169-25
169-26
169-27
169-28
169-29
169-30
169-31
169-32
169-33
169-34
169-35
169-36
169-37
169-38
169-39
169-40
169-41
UDI:
10885403512704
10885403517167
10885403517181
10885403512568
10885403512544

Quantity affected: 2679 units.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96029
Status: Active
Manufacturer: CareFusion 303, Inc.
Sold By: Medical facilities; Hospitals
Manufactured In: United States
Units Affected: 2679
Distributed To: Kansas, Texas, California, Pennsylvania, New Jersey, Florida, Indiana, Arizona, Illinois, Massachusetts, New York, Kentucky, Utah, Maryland, Washington, Ohio, Alabama

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.