PlainRecalls
FDA Devices Moderate Class II Terminated

Cios Alpha VA20/ VA30 mobile X-Ray systems

Reported: July 17, 2019 Initiated: June 20, 2019 #Z-1953-2019

Product Description

Cios Alpha VA20/ VA30 mobile X-Ray systems

Reason for Recall

DAP chamber may be missing an insulating foil

Details

Units Affected
1
Distribution
IL, NE
Location
Malvern, PA

Frequently Asked Questions

What product was recalled?
Cios Alpha VA20/ VA30 mobile X-Ray systems. Recalled by Siemens Medical Solutions USA, Inc. Units affected: 1.
Why was this product recalled?
DAP chamber may be missing an insulating foil
Which agency issued this recall?
This recall was issued by the FDA Devices on July 17, 2019. Severity: Moderate. Recall number: Z-1953-2019.