BD Pyxis MedStation ES AUX — Class II medical device recall Z-0972-2025
Ongoing recall by CareFusion 303, Inc., reported 2025-01-29. Drawer and/or door failures that may lead to a delay in access to medications. The following three situations
| Recall number | Z-0972-2025 |
|---|---|
| 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 | 2023-02-14 |
| Classified | 2025-01-17 |
| Reported by FDA | 2025-01-29 |
| Quantity | 39,615 units |
| UPC / GTIN / UDI-DI | 10885403512681 |
| Serial numbers | 12440840, 12440841, 12448207, 12448208, 12452252, 12452264, 12455476, 12457600, 12457601, 12462734, 12462735, 12463676, 12468607, 12468608, 12468609, 12468610, 12468611, 12468612, 12468670, 12468671, 12468672, 12468673, 12468674, 12473807, 12473808 and 475 more |
| Model numbers | 324 |
Product
BD Pyxis MedStation ES AUX, REF 324
Reason for recall
Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,
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-0972-2025. 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.