Mobilett Mira wireless — Class II medical device recall Z-0223-2024
Ongoing recall by Siemens Medical Solutions USA, Inc, reported 2023-11-22, distributed nationwide. Due to the incorrect mounting of the buzzer component, there is no acoustic signal during x ray activation. Ot
| Recall number | Z-0223-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | FDA mandated |
| Recalling firm | Siemens Medical Solutions USA, Inc, Malvern, PA, United States |
| Recall initiated | 2023-10-05 |
| Classified | 2023-11-14 |
| Reported by FDA | 2023-11-22 |
| Distributed | Nationwide (US) |
| Quantity | 4 distributed |
| UPC / GTIN / UDI-DI | 04056869009117 |
| Serial numbers | 1511, 2168, 2525, 2633 |
| Model numbers | 10273100 |
Product
Mobilett Mira wireless (VA20) mobile x-ray system(s)
Reason for recall
Due to the incorrect mounting of the buzzer component, there is no acoustic signal during x ray activation. Otherwise, the system is fully functional, and x ray is applied correctly. By means of the additional visual indicator (exposure LED light) the operator can monitor the x ray release. Also, after a successful x ray exposure, the clinical image is displayed on the monitor.
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-0223-2024. 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.