Various models of BD Pyxis Pro 7-Drawer Auxiliary, Reference numbers: 1149-00 and 1152-00
FDA Recall Z-0369-2026 · Posted 2025-10-27
Recalling FirmCareFusion 303, Inc.
Recall StatusOpen, Classified
Product CodeBRY
Date Initiated2025-09-30
Product Quantity32 units
Reason for Recall
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Firm Action
On September 30, 2025, BD issue a Urgent Medical Device Recall Expansion notification to affected consignees via FedEx. BD is asking consignees to take the following actions:
1. Affected products can continue to be used per existing Manuals and Guides.
2. In the event of an accidental fluid spill on the device or in a drawer, users should following instructions outlined within the customer notification.
3. Review the customer letter attachment which provides warnings, cautions and recommendations regarding fluid ingress.
4. Complete the attached Customer Response Form and return to the BD contact noted on the form whether or not you have any of the impacted material.
Root Cause
Under Investigation by firm
Distribution Pattern
Worldwide distribution - US Nationwide and the countries of Canada, United Arab Emirates, Australia.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.