FDA Medical devices recall ·
BD Pyxis Pro MedStation Main recall
- Recall number
- Z-0370-2026
- Date
- (initiated September 30, 2025)
- Company / brand
- CareFusion 303, Inc.
10020 Pacific Mesa Blvd, San Diego, CA, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 27 units
- Hazard tags
- Fire
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
BD Pyxis Pro MedStation Main, REF: 1155-00
Why was it recalled?
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
All Serial Numbers/Ref #/UDI: 1155-00 10885403521300
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, United Arab Emirates, Australia.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-0370-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.