Luminos dRF Max- Intended to visualize anatomical structures by… — Class II medical device recall Z-2526-2024
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-2526-2024 |
|---|---|
| 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 | 24 units |
| Serial numbers | 5615, 5664, 7136, 7791, 7805, 8093, 8095, 8130, 8150, 8183, 8198, 8244, 8300, 8320, 8322, 8334, 8371, 8378, 8436, 8468, 8474, 8479, 8613, 8660 |
| Model numbers | 10762471 |
Product
Luminos dRF Max- Intended to visualize anatomical structures by converting an x-ray pattern into a visible image. Model Number: 10762471
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-2526-2024. 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.