FDA Device recall Z-1785-2022
BD Pyxis MedBank Cabinet Software v2.1.2.9 Legacy MedBank Cabinets with Matrix Drawers include: . CUBEX MedFlex operating with Windows 7 .…
- FDA Device
- Class II
- ongoing
- Published 2022-10-05
On 2022-10-05 the FDA classified a Class II recall of BD Pyxis MedBank Cabinet Software v2.1.2.9 Legacy MedBank Cabinets with Matrix Drawers include: . CUBEX MedFlex operating with Windows 7 .… by Carefusion 303, citing the automated dispensing cabinet software update included a .dll file that is not compatible with MedBank Cabinet stations with MedCart Matrix drawers. The cabinet system will sto….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1785-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-05-24 |
| Published | 2022-10-05 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Carefusion 303 |
| Distribution | US |
Product
BD Pyxis MedBank Cabinet Software v2.1.2.9 Legacy MedBank Cabinets with Matrix Drawers include: . CUBEX MedFlex operating with Windows 7 . MedBank 200 Main operating with Windows 7 . MedBank 500 Main operating with Windows 7. An automated dispensing cabinet intended to securely store and dispense medications to health care providers in a clinical setting.
Reason
The automated dispensing cabinet software update included a .dll file that is not compatible with MedBank Cabinet stations with MedCart Matrix drawers. The cabinet system will stop functioning (Matrix drawers will stop opening in the MedBank Application) leading to delay in access to medications or supplies needed in residential or procedural care facilities.
Identifiers
| code_info | Software Version - v2.1.2.9 UDI Code: N/A Cabinet System Serial Numbers containing the affected software: 14473379 152…Software Version - v2.1.2.9 UDI Code: N/A Cabinet System Serial Numbers containing the affected software: 14473379 15268856 14728142 15080054 14891492 15216161 13819501 14443828 14443829 14443838 14461825 14461827 14461829 14461830 14461836 14461838 14461840 14461842 14461843 14461845 14461848 14473356 14473359 14473371 14473376 14473377 14491507 14491510 14491511 14491513 14491514 14491516 14491518 14491519 14491523 14491524 14491526 14491529 14491533 14491534 14491535 14491536 14491537 14509122 14509123 14509124 14509126 14509128 14509130 14509136 14509137 14509138 14509139 14509141 14531591 14532282 14532284 14532285 14532286 14532287 14532290 14532294 14532295 14532298 14532299 14532300 14532301 14532302 14568029 14568034 14568035 14568036 14568037 14568038 14568041 14568042 14568045 14568046 14568050 14568054 14603154 14607364 14607368 14607369 14649246 14699416 14532304 14568027 14461834 14491520 14491522 14532288 14532292 14532305 14491512 14532297 14443834 14532293 14532291 14 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1785-2022%22
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