FDA Device recall Z-2525-2024
Luminos Agile 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 Agile 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-2525-2024 |
| 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 Agile Max -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image. Model Number: 10762472
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: (01)04056869009162(21) Serial Numbers; Serial Number 64144 61058 64374 64413 64433 64048 64460 64385 64036 64013 6…UDI: (01)04056869009162(21) Serial Numbers; Serial Number 64144 61058 64374 64413 64433 64048 64460 64385 64036 64013 64448 64451 64445 64057 64205 64326 64055 64051 64262 64288 64338 64061 64131 64314 64399 64034 64443 64105 64019 64309 64325 61231 64032 64170 64088 64457 64478 64104 64244 64449 64316 64111 64280 64239 64241 64420 64412 64136 64273 64112 64247 64329 64124 64486 64196 64320 64388 64147 64446 64479 64290 64299 64397 64228 64117 64176 64327 64251 64098 64060 64441 64452 64100 64313 64082 64041 64035 64029 64110 64381 63388 64278 64444 64078 64191 64435 64331 64174 64377 64426 64300 64118 64333 64127 64257 64348 64281 64211 64382 64271 64149 64346 64464 64266 64199 64431 64179 64336 64396 64099 64090 64107 64172 64469 64180 64364 63386 64384 64238 64305 64484 64311 64221 64285 64204 64265 64408 64383 64154 64103 64483 64407 64470 64248 64021 64418 64334 64276 64252 64400 64120 64083 64150 64129 64053 64089 64058 64145 64141 64073 64347 64332 64471 64185 64193 64390 64393 |
|---|
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-2525-2024%22
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