FDA Device recall Z-0928-2023
BD Pyxis MedBank System - Product Label/labeling pending
- FDA Device
- Class II
- ongoing
- Published 2023-01-18
On 2023-01-18 the FDA classified a Class II recall of BD Pyxis MedBank System - Product Label/labeling pending by Carefusion 303, citing due to customer complaints related to the MedBank software which may indicate that a different medication is loaded in a cubie (drawer) pocket than what is physically loaded and l….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0928-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-12-12 |
| Published | 2023-01-18 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Carefusion 303 |
| Distribution | US |
Product
BD Pyxis MedBank System - Product Label/labeling pending
Reason
Due to customer complaints related to the MedBank software which may indicate that a different medication is loaded in a cubie (drawer) pocket than what is physically loaded and listed on the pocket label. As a result of this issue, a patient could receive the wrong medication or wrong dose of medication that could lead to patient harm.
Identifiers
| code_info | BD Pyxis" MedBank Tower Main UDI Code: 10885403512568 Catalog Numbers: 169-23 to 169-81, 169-100, 169-132, 169-138, 169…BD Pyxis" MedBank Tower Main UDI Code: 10885403512568 Catalog Numbers: 169-23 to 169-81, 169-100, 169-132, 169-138, 169-139 BD Pyxis" MedBank Mini Main UDI Code: 10885403512544 Catalog Numbers: 169-101 - 169-113, 169-137 BD Pyxis" MEDFLEX BD Pyxis" MEDFLEX 2.0 UDI Codes:10885403512704 Catalog Numbers: 1119-00 1139-00 MedBank 200/500 UDI Code: N/A Catalog Numbers: 1137-00 BD Pyxis MEDPASS v1.0 or prior UDI Code: 10885403513817 Catalog Number: Not Provided BD Pyxis" MedBank Cabinet Software v2.2 or prior UDI Codes: 10885403513794 Catalog Number: N/A Affected Serial Numbers: 12940473 12971999 12972001 12972004 12972006 12972007 12982486 12982487 12982488 12982489 12982490 12982491 12982492 12982493 13517006 13523350 13598718 13629024 13727050 13739164 13754724 13766710 13766711 13767953 13769979 13770265 13770291 13789575 13792769 13801727 13802400 13817034 13819501 13826187 13829362 13829363 13829364 13832440 13843251 13849951 13853916 13853918 13856246 13873024 13875126 13875127 1 |
|---|
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-0928-2023%22
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