FDA Device recall Z-2526-2024
Luminos dRF Max- Intended to visualize anatomical structures by converting an x-ray pattern into a visible image
- FDA Device
- Class II
- ongoing
- Published 2024-08-14
On 2024-08-14 the FDA classified a Class II recall of Luminos dRF Max- Intended to visualize anatomical structures by converting an x-ray pattern into a visible image by Siemens Medical Solutions Usa, citing the support arm may unintentionally lower resulting in injury to persons when they are under the display ceiling/wall suspension when positioning the displays.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2526-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-07-02 |
| Published | 2024-08-14 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
Luminos dRF Max- Intended to visualize anatomical structures by converting an x-ray pattern into a visible image. Model Number: 10762471
Reason
The support arm may unintentionally lower resulting in injury to persons when they are under the display ceiling/wall suspension when positioning the displays
Identifiers
| code_info | UDI: Serial Numbers: Serial Number 8320 8198 8334 8474 8183 8322 8613 8244 8660 8436 8095 8371 8378 7805 5664 5615 8150 8130 8300 8093 8468 7791 8479 7136 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2526-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.