CareFusion 303, Inc. 2025-12-31 Health serious FDA
Health · FDA · Recall #FDA-Z-0962-2026
BD Pyxis MedStation ES, REF: 323, BD Pyxis MedStation ES 7 Drawer Auxiliary, REF: 324,… Recall
Issued December 31, 2025 · CareFusion 303, Inc.
In December 2025, CareFusion 303, Inc. recalled the BD Pyxis MedStation ES, REF: 323, BD Pyxis MedStation ES 7 Drawer Auxiliary, REF: 324,…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer firmware update, which caused a Cubie Insert event which prompts software to generate a duplicate address, which causes an error and the drawer to fail, which may lead to inability or delay in accessing stored items, delay in the replenishment of ADCs or patient specific medications stored outside of ADCs.
What you should do
- 1 Stop using BD Pyxis MedStation ES, REF: 323, BD Pyxis MedStation ES 7 Drawer Auxiliary, REF: 324,… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact CareFusion 303, Inc. to arrange your voluntary. See the official notice below for contact details.
- 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
- December 31, 2025
- Units affected
- Not reported
- Sold at
- Worldwide - US Nationwide distribution including in the states of CO, IN, OH, TX, KS, FL, GA, NC, CA, HI, IL, NY, MI, VA, AL, LA, NE, KY, O
- Recall number
- FDA-Z-0962-2026
- 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 691st Health recall we've logged in 2025.