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CareFusion 303, Inc. recalls BD Pyxis Pro MedStation Main, REF: 1155-00
Recalled November 5, 2025 · FDA recall Z-0370-2026 · CareFusion 303
Hazard
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire. · FDA Class II
Units
27 units
Sold at
Worldwide distribution - US Nationwide and the countries of Canada, United Arab Emirates, Australia.
Description
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Product
BD Pyxis Pro MedStation Main, REF: 1155-00
Manufacturer(s)
CareFusion 303, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →