Siemens Mobilett Mira mobile x-ray system Product Usage: Mobile x-ray… — Class II medical device recall Z-2367-2012
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2012-09-19, distributed nationwide. During regular product monitoring, firm became aware of a potential issue with the Mobilett Mira system, (seri
| Recall number | Z-2367-2012 |
|---|---|
| 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 | 2012-04-30 |
| Classified | 2012-09-11 |
| Reported by FDA | 2012-09-19 |
| Terminated | 2012-09-25 |
| Distributed | Nationwide (US) |
| Quantity | 9 |
| Serial numbers | 1034, 1038, 1041, 1042, 1043, 1050, 1053, 1054 |
| Model numbers | 10273100 |
Product
Siemens Mobilett Mira mobile x-ray system Product Usage: Mobile x-ray system
Reason for recall
During regular product monitoring, firm became aware of a potential issue with the Mobilett Mira system, (serial numbers 1034, 1038, 1041, 1042, 1043, 1050, 1053, and 1054. During normal clinical operation the center screw on the driving wheel may become loose resulting in system immobilization. There is no risk of the system tipping over or collapsing on the floor, however the system may tilt t
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-2367-2012. 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.