Luminos Agile Max -Intended to visualize anatomical structures by… — Class II medical device recall Z-2525-2024
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-2525-2024 |
|---|---|
| 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 | 333 units |
| UPC / GTIN / UDI-DI | 04056869009162 |
| Serial numbers | 61058, 61231, 63372, 63382, 63386, 63388, 64012, 64013, 64015, 64018, 64019, 64021, 64022, 64027, 64028, 64029, 64031, 64032, 64034, 64035, 64036, 64039, 64040, 64041, 64043 and 308 more |
| Model numbers | 10762472 |
Product
Luminos Agile Max -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image. Model Number: 10762472
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-2525-2024. 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.