FDA recall Z-0369-2026

CareFusion 303, Inc. · Class II · device

Product

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.

Distribution

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

Key facts

Status
Ongoing
Initiation date
2025-09-30
Report date
2025-11-05
Voluntary/Mandated
Voluntary: Firm initiated
Location
San Diego, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0369-2026