Mobiletta Mira Mobile X-ray System — Class II medical device recall Z-1875-2013
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2013-08-14, distributed in AR, GA, IA, ID, IL, KS, MI, NC…. Siemens issued a Field Safety Alert about the potential risk to users when operating the Mobilett Mira. When a
| Recall number | Z-1875-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Medical Solutions USA, Inc, Malvern, PA, United States |
| Recall initiated | 2013-05-02 |
| Classified | 2013-08-05 |
| Reported by FDA | 2013-08-14 |
| Terminated | 2015-02-24 |
| Distributed | AR, GA, IA, ID, IL, KS, MI, NC, NE, OH, SD, TX, WI |
| Quantity | 39 |
| Reason classes | device malfunction |
| Model numbers | 10273100 |
Product
Mobiletta Mira Mobile X-ray System
Reason for recall
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
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-1875-2013. 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.