Class II

Medical Device Recall: BD Pyxis Pro MedStation Main, REF: 1155-00

CareFusion 303, Inc. · September 30, 2025

Reason for Recall

Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.

Distribution

Worldwide distribution - US Nationwide and the countries of Canada, United Arab Emirates, Australia.

States Affected

NATIONWIDE

Quantity Affected

27 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0370-2026

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.

CareFusion 303, Inc. Medical Device Recall: BD Pyxis Pro MedStation Main, REF: 1155-00 | SafeCheck