FDA Device recall Z-2300-2026
BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet
- FDA Device
- Class II
- ongoing
- Published 2026-06-10
On 2026-06-10 the FDA classified a Class II recall of BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet by Carefusion 303, citing fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2300-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-04-30 |
| Published | 2026-06-10 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Carefusion 303 |
| Distribution | US |
Product
BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet
Reason
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Identifiers
| code_info | All Serial Numbers/UDI:10885403477829 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2300-2026%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.