FDA Device recall Z-0671-2025
BD Pyxis MedStation ES 7 Drawer Auxiliary Tower, REF: 324
- FDA Device
- Class II
- ongoing
- Published 2024-12-18
On 2024-12-18 the FDA classified a Class II recall of BD Pyxis MedStation ES 7 Drawer Auxiliary Tower, REF: 324 by Carefusion 303, citing due to a software issue, automated dispensing cabinet devices may open the wrong cubie pocket or position, which can lead to: 1) Unintended and incorrect medication removal, or 2)….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0671-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-11-14 |
| Published | 2024-12-18 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Carefusion 303 |
| Distribution | US |
Product
BD Pyxis MedStation ES 7 Drawer Auxiliary Tower, REF: 324
Reason
Due to a software issue, automated dispensing cabinet devices may open the wrong cubie pocket or position, which can lead to: 1) Unintended and incorrect medication removal, or 2) Potential for a different medication (medication pulled in error) to be refilled/loaded, which may lead to may lead to low inventory or a stockout.
Identifiers
| code_info | All software versions. REF/UDI-DI: 324/10885403512681/ 12440840 12440841 12448208 12452252 12452264 12455476 12462734…All software versions. REF/UDI-DI: 324/10885403512681/ 12440840 12440841 12448208 12452252 12452264 12455476 12462734 12462735 12463676 12468609 12468612 12468607 12468608 12468610 12468671 12468672 12468674 12468670 12468673 12468611 12474015 12474022 12473810 12473813 12473815 12473816 12473817 12473811 12473921 12474012 12474071 12474014 12473887 12473922 12474013 12473807 12473812 12473808 12473809 12476548 12495456 12499285 12502858 12502857 12503069 12508589 12508584 12508578 12508579 12508587 12508580 12510555 12510559 12510393 12520264 12520266 12520267 12520269 12528519 12528411 12530586 12530588 12530589 12530587 12531133 12531132 12532495 12532494 12532490 12532491 12532493 12532492 12533583 12533588 12533589 12533562 12533563 12533561 12533584 12533587 12533585 12533586 12533259 12533261 12533262 12533263 12534455 12534456 12534461 12540265 12540264 12544944 12546962 12547840 12547841 12549213 12552380 12552381 12553970 12553971 12553972 12553973 12553558 12553773 12553559 |
|---|
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-0671-2025%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.