FDA Device recall Z-1875-2013
Mobiletta Mira Mobile X-ray System
- FDA Device
- Class II
- terminated
- Published 2013-08-14
On 2013-08-14 the FDA classified a Class II recall of Mobiletta Mira Mobile X-ray System by Siemens Medical Solutions Usa, citing siemens issued a Field Safety Alert about the potential risk to users when operating the Mobilett Mira. When a Mobilett Mira is regularly exposed to extensive mechanical strain (d….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1875-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-05-02 |
| Published | 2013-08-14 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | AR, GA, IA, ID, IL, KS, MI, NC, NE, OH, SD, TX, WI |
Product
Mobiletta Mira Mobile X-ray System
Reason
Siemens issued a Field Safety Alert about the potential risk to users when operating the Mobilett Mira. When a Mobilett Mira is regularly exposed to extensive mechanical strain (driven over high thresholds for doors or elevators), it is possible that one of its main wheel shafts could break because of material fatigue, resulting in the chassis falling on the ground on the affected wheel side. This
Identifiers
| code_info | Model number 10273100 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1875-2013%22
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