Medical Device Recall: (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
CareFusion 303, Inc. · January 8, 2025
Reason for Recall
Labeling is insufficient regarding delays in access to medication. The firm is strengthening the label as an additional risk mitigation.
Product Description
(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
Distribution
Domestic distribution nationwide US. International distribution to North America, Latin America, EMEA, and Greater Asia.
States Affected
NATIONWIDE
Quantity Affected
193067
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1120-2025
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.