Class II

Medical Device Recall: (1) Pyxis MedStation ES, Catalog No. 323; (2) Pyxis Anesthesia Station (PAS), Catalog No. 327; (3) Pyxis MedStation ES Tower, Catalog No. 352; (4) BD Pyxis CII Safe ES, Catalog No. 1116-00

CareFusion 303, Inc. · January 8, 2025

Reason for Recall

Software issues could potentially result in: 1) delays in accessing dispensing software application, 2) wrong therapy (dose, item, timing, etc.), or 3) unauthorized access and/or compliance related issues

Distribution

Domestic distribution nationwide. International distribution to North America, Latin America, EMEA, and Greater Asia.

States Affected

NATIONWIDE

Quantity Affected

137,741 total

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1119-2025

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.