Recall Z-0369-2026— CareFusion 303, Inc.

Name: FDA recall Z-0369-2026
Creator: U.S. Food and Drug Administration
Published: 2025-09-30

Class II · Ongoing

Class II FDA medical device recall by CareFusion 303, Inc., initiated 2025-09-30. FDA's recall record names no specific 510(k) clearance for this event. Product: Various models of BD Pyxis Pro 7-Drawer Auxiliary, Reference numbers: 1149-00 and 1152-00. Reason: Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire..

Recalling firm: CareFusion 303, Inc.
Classification: Class II
Status: Ongoing
Initiated: 2025-09-30
Firm location: San Diego, CA, United States

Product description

Various models of BD Pyxis Pro 7-Drawer Auxiliary, Reference numbers: 1149-00 and 1152-00

Reason for recall

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

Data sourced from openFDA. This site is unofficial and independent of the FDA.