FDA Device recall Z-0371-2026
All Serial Numbers/BD Pyxis CII Safe ES Tower Main, REF: 1116-00
- FDA Device
- Class II
- ongoing
- Published 2025-11-05
On 2025-11-05 the FDA classified a Class II recall of All Serial Numbers/BD Pyxis CII Safe ES Tower Main, REF: 1116-00 by Carefusion 303, citing potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0371-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-09-30 |
| Published | 2025-11-05 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Carefusion 303 |
| Distribution | US |
Product
All Serial Numbers/BD Pyxis CII Safe ES Tower Main, REF: 1116-00
Reason
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Identifiers
| code_info | Ref #/UDI: 1116-00 10885403512605 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0371-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.