FDA Device recall Z-1953-2019
Cios Alpha VA20/ VA30 mobile X-Ray systems
- FDA Device
- Class II
- terminated
- Published 2019-07-17
On 2019-07-17 the FDA classified a Class II recall of Cios Alpha VA20/ VA30 mobile X-Ray systems by Siemens Medical Solutions Usa, citing DAP chamber may be missing an insulating foil.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1953-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-06-20 |
| Published | 2019-07-17 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | IL, NE |
Product
Cios Alpha VA20/ VA30 mobile X-Ray systems
Reason
DAP chamber may be missing an insulating foil
Identifiers
| code_info | Material # 10308191 Serial # 13161 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1953-2019%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.