CareFusion 303, Inc.: Medical Device Recall in 2025 - (Recall #: Z-0369-2026)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: September 30, 2025

Date Posted: November 5, 2025

Recall Number: Z-0369-2026

Event ID: 97566

Reason for Recall:

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

Status: Ongoing

Product Quantity: 32 units

Code Information:

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

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated