FDA Device recall Z-0962-2026
BD Pyxis MedStation ES, REF: 323, BD Pyxis MedStation ES 7 Drawer Auxiliary, REF: 324, BD Pyxis MedStation ES Tower, REF: 352, BD Pyxis Pro…
- FDA Device
- Class II
- ongoing
- Published 2025-12-31
On 2025-12-31 the FDA classified a Class II recall of BD Pyxis MedStation ES, REF: 323, BD Pyxis MedStation ES 7 Drawer Auxiliary, REF: 324, BD Pyxis MedStation ES Tower, REF: 352, BD Pyxis Pro… by Carefusion 303, citing automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer firmware update, which caused a Cubie Insert event which prompts software to generate a duplicate address,….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0962-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-11-20 |
| Published | 2025-12-31 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Carefusion 303 |
| Distribution | US |
Product
BD Pyxis MedStation ES, REF: 323, BD Pyxis MedStation ES 7 Drawer Auxiliary, REF: 324, BD Pyxis MedStation ES Tower, REF: 352, BD Pyxis Pro 7-Drawer Auxiliary, REF: 1149-00, BD Pyxis Pro 7- Drawer Auxiliary with Secure Tower, REF: 1152-00, BD Pyxis Pro MedStation Main, REF: 1155-00, BD Pyxis CII Safe ES, REF: 1116-00
Reason
Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer firmware update, which caused a Cubie Insert event which prompts software to generate a duplicate address, which causes an error and the drawer to fail, which may lead to inability or delay in accessing stored items, delay in the replenishment of ADCs or patient specific medications stored outside of ADCs.
Identifiers
| code_info | Firmware Version: 1.48. REF/UDI-DI: 323/10885403512667, 324/10885403512681, 352/10885403512674, 1149-00/10885403517822,…Firmware Version: 1.48. REF/UDI-DI: 323/10885403512667, 324/10885403512681, 352/10885403512674, 1149-00/10885403517822, 1152-00/10885403517839, 1155-00/10885403521300, 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.
Other recalls by Carefusion 303
- BD Pyxis MedStation ES Tower REF: 352 Medication cabinet
FDA Device · Class II · 2026-06-10 · Carefusion 303 - BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet
FDA Device · Class II · 2026-06-10 · Carefusion 303 - BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet
FDA Device · Class II · 2026-06-10 · Carefusion 303 - BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet
FDA Device · Class II · 2026-06-10 · Carefusion 303 - BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet
FDA Device · Class II · 2026-06-10 · Carefusion 303
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0962-2026%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.