FDA Medical Device Recalls (openFDA)
Siemens Medical Solutions USA, Inc: Cios Alpha VA20/ VA30 mobile X-Ray systems
- Recall number
- Z-1953-2019
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Product
- Cios Alpha VA20/ VA30 mobile X-Ray systems
- Status
- Terminated
- Initiated
- 2019-06-20
- Posted
- not on file
- Terminated
- 2020-04-17
- Reason
- DAP chamber may be missing an insulating foil
- Root cause
- Nonconforming Material/Component
- Action
- 1. Siemens will inspect the DAP chamber on your unit, and if necessary, replace it with insulated DAP chamber. 2. Siemens service organization will contact you shortly to arrange a date to perform this corrective action. 3. Please feel free to contact our service organization for an earlier appointment at 1-800-888-7436.
- Quantity
- 1
- Distribution
- IL, NE
- Lot, serial or model codes
- Material # 10308191 Serial # 13161
- 510(k) numbers
- ["K132094","K181560"]
- PMA numbers
- not on file
- Product code
- OWB
- Firm FEI
- 2240869
- Firm city
- Malvern
- Firm state
- PA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28