BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P — Class II medical device recall Z-2503-2024
Ongoing recall by CareFusion 303, Inc., reported 2024-08-14, distributed nationwide. Due to software issue, there is a potential when a restock label is printed for a medication stored in automat
| Recall number | Z-2503-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | CareFusion 303, Inc., San Diego, CA, United States |
| Recall initiated | 2024-06-24 |
| Classified | 2024-08-02 |
| Reported by FDA | 2024-08-14 |
| Distributed | Nationwide (US) |
| Quantity | 16 units |
| Reason classes | labeling, software |
| UPC / GTIN / UDI-DI | 10885403512568 |
| Serial numbers | 15631124, 15632972, 15815836, 15937573, 16073534, 16095341, 16097230, 16101319, 16112043, 16173241, 16184767, 16209953, 16209954, 16210468, 16232272, 16274000 |
| Model numbers | 169-99 |
Product
BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P, REF: 169-99 containing software version 3.9.1.9
Reason for recall
Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2503-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.