CareFusion 303, Inc. recalls BD Pyxis Pro MedStation Main
- Recalling company
- CareFusion 303, Inc.
- Product
- BD Pyxis Pro MedStation Main, REF: 1155-00
- Reason
- Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Sep 30, 2025
- Reported
- Nov 5, 2025
- Distribution
- Worldwide distribution - US Nationwide and the countries of Canada, United Arab Emirates, Australia.
- Status
- Ongoing
- Quantity
- 27 units
- Lot / codes
- All Serial Numbers/Ref #/UDI: 1155-00 10885403521300
- Company location
- San Diego, CA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0370-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0370-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.