Cios Alpha VA20/ VA30 mobile X-Ray systems recall
Cios Alpha VA20/ VA30 mobile X-Ray systems
Why was Cios Alpha VA20/ VA30 mobile X-Ray systems recalled?
DAP chamber may be missing an insulating foil
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Material # 10308191 Serial # 13161
- Product
- Cios Alpha VA20/ VA30 mobile X-Ray systems
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 1
- Distribution
- IL, NE
- Recall date
- July 17, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)