LUMINOS Lotus Max -Intended to visualize anatomical structures by… — Class II medical device recall Z-2527-2024
Ongoing recall by Siemens Medical Solutions USA, Inc, reported 2024-08-14, distributed nationwide. The support arm may unintentionally lower resulting in injury to persons when they are under the display ceili
| Recall number | Z-2527-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Medical Solutions USA, Inc, Malvern, PA, United States |
| Recall initiated | 2024-07-02 |
| Classified | 2024-08-07 |
| Reported by FDA | 2024-08-14 |
| Distributed | Nationwide (US) |
| Quantity | 26 units |
| UPC / GTIN / UDI-DI | 04056869269931 |
| Serial numbers | 10024, 10029, 10030, 10063, 10073, 10076, 10079, 10091, 10115, 10117, 10140, 10170, 10172, 10173, 10181, 10194, 10234, 10251, 10253, 10274, 10278, 10307, 10309, 10311, 10327 and 1 more |
| Model numbers | 11574100 |
Product
LUMINOS Lotus Max -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image Model Number: 11574100
Reason for recall
The support arm may unintentionally lower resulting in injury to persons when they are under the display ceiling/wall suspension when positioning the displays
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-2527-2024. 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.