FDA Device recall Z-2367-2012
Siemens Mobilett Mira mobile x-ray system Product Usage: Mobile x-ray system
- FDA Device
- Class II
- terminated
- Published 2012-09-19
On 2012-09-19 the FDA classified a Class II recall of Siemens Mobilett Mira mobile x-ray system Product Usage: Mobile x-ray system by Siemens Medical Solutions Usa, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2367-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-04-30 |
| Published | 2012-09-19 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
Siemens Mobilett Mira mobile x-ray system Product Usage: Mobile x-ray system
Reason
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
Identifiers
| code_info | Model number 10273100 - serial numbers 1034, 1038, 1041, 1042, 1043, 1050, 1053, and 1054 |
|---|
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-2367-2012%22
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