Various models of BD Pyxis Pro 7-Drawer Auxiliary, Reference numbers: 1149-00 and 1152-00
Reported: November 5, 2025 Initiated: September 30, 2025 #Z-0369-2026
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.
Details
- Recalling Firm
- CareFusion 303, Inc.
- Units Affected
- 32 units
- Distribution
- Worldwide distribution - US Nationwide and the countries of Canada, United Arab Emirates, Australia.
- Location
- San Diego, CA
Frequently Asked Questions
What product was recalled? ▼
Various models of BD Pyxis Pro 7-Drawer Auxiliary, Reference numbers: 1149-00 and 1152-00. Recalled by CareFusion 303, Inc.. Units affected: 32 units.
Why was this product recalled? ▼
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 5, 2025. Severity: Moderate. Recall number: Z-0369-2026.
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