FDA Device recall Z-2947-2024
BD Pyxis QFill Replenishment Station, REF: 138904-01, medication cabinet system
- FDA Device
- Class II
- ongoing
- Published 2024-09-11
On 2024-09-11 the FDA classified a Class II recall of BD Pyxis QFill Replenishment Station, REF: 138904-01, medication cabinet system by Carefusion 303, citing due to software issue, there is a potential when a restock label is printed for a medication stored in a non-CUBIE location, that the incorrect bin for the medication is printed o….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2947-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-07-09 |
| Published | 2024-09-11 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Carefusion 303 |
| Distribution | US |
Product
BD Pyxis QFill Replenishment Station, REF: 138904-01, medication cabinet system
Reason
Due to software issue, there is a potential when a restock label is printed for a medication stored in a non-CUBIE location, that the incorrect bin for the medication is printed on the label.
Identifiers
| code_info | serial numbers: 44210411, 43880801, 44227426/ UDI: None |
|---|
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-2947-2024%22
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