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CareFusion 303, Inc. recalls (1) BD Pyxis MedStation ES, Catalog No. 323; (2) BD Pyxis Anesthesia Station (PAS), Catalog No. 327; (3) BD Pyxis MedSta
Recalled February 19, 2025 · FDA recall Z-1120-2025 · CareFusion 303
Hazard
Labeling is insufficient regarding delays in access to medication. The firm is strengthening the label as an additional risk mitigation. · FDA Class II
Units
193067
Sold at
Domestic distribution nationwide US. International distribution to North America, Latin America, EMEA, and Greater Asia.
Description
Labeling is insufficient regarding delays in access to medication. The firm is strengthening the label as an additional risk mitigation.
Product
(1) BD Pyxis MedStation ES, Catalog No. 323; (2) BD Pyxis Anesthesia Station (PAS), Catalog No. 327; (3) BD Pyxis MedStation ES Tower, Catalog No. 352; (4) BD Pyxis MedStation 4000 Console, Catalog No. 309; (5) BD Pyxis MedStation 4000, Catalog No. 303; (6) BD Pyxis Anesthesia System 4000, Catalog No. 338
Manufacturer(s)
CareFusion 303, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →