CareFusion 303, Inc. 2025-10-15 Health critical FDA
Health · FDA · Recall #FDA-Z-0035-2026
BD Alaris Pump Infusion Sets for the following reference numbers: C24101E, Amber… Recall
Issued October 15, 2025 · CareFusion 303, Inc.
In October 2025, CareFusion 303, Inc. recalled the BD Alaris Pump Infusion Sets for the following reference numbers: C24101E, Amber…, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time to alarm, and post-occlusion bolos volume.
What you should do
- 1 Stop using BD Alaris Pump Infusion Sets for the following reference numbers: C24101E, Amber… 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
- October 15, 2025
- Units affected
- Not reported
- Sold at
- US: Nationwide OUS: United Arab Emirates Australia Belgium Bahrain Botswana Canada Switzerland China France United Kingdom Gibraltar
- Recall number
- FDA-Z-0035-2026
- 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.