Class II — CareFusion 303, Inc.
| Recalling firm | CareFusion 303, INC. |
|---|---|
| Registered facility | View this company's 3 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire. |
| Product | BD Pyxis Pro MedStation Main, REF: 1155-00 |
| Quantity | 27 units |
| Distribution | Worldwide distribution - US Nationwide and the countries of Canada, United Arab Emirates, Australia. |
| Initiated | 2025-09-30 |
| Classified | 2025-10-27 |
| Recall number | Z-0370-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — CareFusion 303, Inc. (Z-0370-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/97566/
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