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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

BD Pyxis ES Enterprise Server Recalled for Software Sync Issue

Agency Publication Date: January 8, 2026
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Summary

CareFusion 303, Inc. is recalling 2,079 BD Pyxis ES Enterprise Server systems due to a software issue that prevents timely updates between the server and hospital systems. The system is used to manage patient, medication, and clinical information for automated dispensing cabinets. This defect can cause clinicians to view outdated patient or medication data, which could lead to errors in medication administration. No injuries have been reported at this time.

Risk

If the software fails to sync information correctly, healthcare providers may use outdated records to dispense medication. This could result in patients receiving the wrong medicine, incorrect dosages, or clinicians being unaware of critical patient updates.

What You Should Do

  1. This recall affects BD Pyxis ES Enterprise Servers with system versions 1.6.1 through 1.11.0 and server application versions ES 4.13 through 5.8.X.
  2. Check the catalog number on your device label; affected units include numbers such as 1115-00, 137672-02, and 137672-03. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled product. Contact the manufacturer or your distributor to arrange return, replacement, or correction.
  4. Contact CareFusion 303, Inc. directly at their San Diego office for further instructions regarding this software update.
  5. Call the FDA: 1-888-463-6332 (1-888-INFO-FDA) for additional information regarding this medical device recall.

Your Remedy Options

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

Affected Products

Product: BD Pyxis ES Enterprise Server
Variants: System Versions 1.6.1 - 1.11.0, Server Application Versions ES 4.13 - 5.8.X, Server Application Versions ES 5.4X - 5.8.X
Model / REF:
1115-00
137672-02
137672-03
137671-02
137671-03
137670-02
137670-03
139676-01
139421-01
139420-01
139419-01
139419-02
139673-01
137081-01
136451-01
136451-02
136450-01
136450-02
136449-01
136449-02
134148-01
133760-01
134149-01
137669-02
137669-03
139675-01
139672-01
139418-01
139418-02
136448-01
136448-02
137673-02
137673-03
139422-01
133744-01
136452-01
136452-02
138551-01
134157-01
UDI:
10885403518348
10885403520341

Recall Number: Z-1028-2026. The BD Pyxis Enterprise Server is a web application intended to configure and manage BD Pyxis ES automated dispensing cabinets.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97546
Status: Active
Manufacturer: CareFusion 303, Inc.
Sold By: Hospitals; Healthcare Facilities; Clinical Institutions
Manufactured In: United States
Units Affected: 2,079 systems
Distributed To: Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Guam, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia, 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.