CareFusion 303 product recalled over fire hazard
- Recall date
- September 30, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- CareFusion 303, Inc. recalls Various models of BD Pyxis Pro 7-Drawer Auxiliary, Reference numbers: 1149-00 and 1152-00
- Recall number
- Z-0369-2026
- FDA classification
- Class II
- Brand / firm
- CareFusion 303, Inc.
- Sold / distributed
- Worldwide distribution - US Nationwide and the countries of Canada, United Arab Emirates, Australia.
Why it was recalled
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Various models of BD Pyxis Pro 7-Drawer Auxiliary, Reference numbers: 1149-00 and 1152-00
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