CareFusion 303, Inc. 2025-01-29 Health serious FDA
Health · FDA · Recall #FDA-Z-0975-2025
BD Pyxis Med ES Auxiliary (AUX), REF 343 Recall
Issued January 29, 2025 · CareFusion 303, Inc.
In January 2025, CareFusion 303, Inc. recalled the BD Pyxis Med ES Auxiliary (AUX), REF 343, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,
What you should do
- 1 Stop using BD Pyxis Med ES Auxiliary (AUX), REF 343 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
- January 29, 2025
- Units affected
- Not reported
- Sold at
- Worldwide
- Recall number
- FDA-Z-0975-2025
- 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.