Z-1953-2019 Class II Terminated
FDA device recall Z-1953-2019 was initiated by Siemens Medical Solutions USA, Inc on June 20, 2019 and is designated Class II. Reason for recall: DAP chamber may be missing an insulating foil The recall status is terminated (terminated April 17, 2020). Affected quantity: 1.
Recall Details
- Product Type
- Devices
- Report Date
- July 17, 2019
- Initiation Date
- June 20, 2019
- Termination Date
- April 17, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1
Product Description
Cios Alpha VA20/ VA30 mobile X-Ray systems
Reason for Recall
DAP chamber may be missing an insulating foil
Distribution Pattern
IL, NE
Code Information
Material # 10308191 Serial # 13161