FDA Device recall Z-0480-2013
Siemens Mobilette Mira, intended use as Mobile x-ray system
- FDA Device
- Class II
- terminated
- Published 2012-12-12
On 2012-12-12 the FDA classified a Class II recall of Siemens Mobilette Mira, intended use as Mobile x-ray system by Siemens Medical Solutions Usa, citing there is a risk of lost images during examination.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0480-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-10-10 |
| Published | 2012-12-12 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
Siemens Mobilette Mira, intended use as Mobile x-ray system.
Reason
There is a risk of lost images during examination.
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-0480-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.