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

FDA Recall #Z-0369-2026 — Class II — September 30, 2025

Recall #Z-0369-2026 Date: September 30, 2025 Classification: Class II Status: Ongoing

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.

Recalling Firm

CareFusion 303, Inc. — San Diego, CA

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

32 units

Distribution

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

Code Information

All Serial Numbers/Ref #/UDI: 1149-00 10885403517822 and 1152-00 10885403517839

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated