FDA recall Z-1953-2019
Siemens Medical Solutions USA, Inc · Class II · device
Product
Cios Alpha VA20/ VA30 mobile X-Ray systems
Reason for recall
DAP chamber may be missing an insulating foil
Distribution
IL, NE
Key facts
- Status
- Terminated
- Initiation date
- 2019-06-20
- Report date
- 2019-07-17
- Termination date
- 2020-04-17
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Malvern, PA, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1953-2019