FDA Device recall Z-2646-2023
BD Pyxis MedBank MedPass Software, REF: 139088-01
- FDA Device
- Class II
- ongoing
- Published 2023-10-04
On 2023-10-04 the FDA classified a Class II recall of BD Pyxis MedBank MedPass Software, REF: 139088-01 by Carefusion 303, citing after dispensing a timed dose medication for a patient, the automated dispensing cabinet software may continue to show the already dispensed medication dose is still available for….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2646-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-08-18 |
| Published | 2023-10-04 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Carefusion 303 |
| Distribution | FL, KS, MI |
Product
BD Pyxis MedBank MedPass Software, REF: 139088-01
Reason
After dispensing a timed dose medication for a patient, the automated dispensing cabinet software may continue to show the already dispensed medication dose is still available for dispense, which could lead to duplicate medication administration.
Identifiers
| code_info | UDI-DI: 10885403513817, Software versions prior to but not including v1.2.3.23 |
|---|
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-2646-2023%22
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