Siemens Mobilette Mira — Class II medical device recall Z-0480-2013
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2012-12-12, distributed nationwide. There is a risk of lost images during examination.
| Recall number | Z-0480-2013 |
|---|---|
| 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 | 2012-10-10 |
| Classified | 2012-12-06 |
| Reported by FDA | 2012-12-12 |
| Terminated | 2014-01-15 |
| Distributed | Nationwide (US) |
| Quantity | 21 |
| Model numbers | 10273100 |
Product
Siemens Mobilette Mira, intended use as Mobile x-ray system.
Reason for recall
There is a risk of lost images during examination.
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-0480-2013. 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.