139088-01 BD PYXIS MEDBANK MEDPASS MODULE 169-151 BD PYXIS MEDBANK… — Class II medical device recall Z-1230-2025
Ongoing recall by CareFusion 303, Inc., reported 2025-03-05, distributed nationwide. Labeling update to include a contraindication statement against the use of medicine cabinets in procedure and
| Recall number | Z-1230-2025 |
|---|---|
| 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 | 2025-01-08 |
| Classified | 2025-02-21 |
| Reported by FDA | 2025-03-05 |
| Distributed | Nationwide (US) |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 10885403503542, 10885403503559, 10885403503566, 10885403503573, 10885403503580, 10885403503597, 10885403503603, 10885403503610, 10885403503658, 10885403503665, 10885403503672, 10885403503689, 10885403503696, 10885403503702, 10885403503719, 10885403503726, 10885403503733, 10885403503740, 10885403503757, 10885403503764, 10885403503771, 10885403503788, 10885403503795, 10885403503801, 10885403503818 and 77 more |
Product
139088-01 BD PYXIS MEDBANK MEDPASS MODULE 169-151 BD PYXIS MEDBANK MINI 1FH-2HH MEDPASS 169-152 BD PYXIS MEDBANK MINI 2HH-1FM MEDPASS 169-150 BD PYXIS MEDBANK MINI 4HH MEDPASS 169-140 BD PYXIS MEDBANK TWR MN 3FH-8HH MEDPASS
Reason for recall
Labeling update to include a contraindication statement against the use of medicine cabinets in procedure and operating rooms.
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-1230-2025. 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.