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Serious recall: Injury is possible or has been reported. Take action promptly.

CareFusion 303, Inc. 2026-01-14 Health serious FDA
Health · FDA · Recall #FDA-Z-1028-2026

BD Pyxis ES Enterprise Server Catalog Numbers 1115-00, 137672-02,137672-03 137671-02,… Recall

Issued January 14, 2026 · CareFusion 303, Inc.

In January 2026, CareFusion 303, Inc. recalled the BD Pyxis ES Enterprise Server Catalog Numbers 1115-00, 137672-02,137672-03 137671-02,…, a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Due a software issue that may result in equipment not receiving timely updates of patient, medication, or related information from enterprise systems.

What you should do

  1. 1 Stop using BD Pyxis ES Enterprise Server Catalog Numbers 1115-00, 137672-02,137672-03 137671-02,… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact CareFusion 303, Inc. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
CareFusion 303, Inc.
Category
Health
Recall date
January 14, 2026
Units affected
Not reported
Sold at
Worldwide - U.S. Nationwide distribution including in the states of AK,AL,AR, AZ, CA, CO, CT, DC, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY
Recall number
FDA-Z-1028-2026
Made in
United States
Issuing agency
FDA

In context

  • CareFusion 303, Inc. has 13 recalls in our database, including 1 rated Critical.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 356th Health recall we've logged in 2026.
Read the official FDA notice

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