Siemens Medical Solutions USA, Inc recalls Cios Alpha VA20/ VA30 mobile X-Ray systems
- Recall date
- June 20, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1953-2019
- FDA classification
- Class II
- Brand / firm
- Siemens Medical Solutions USA, Inc
- Sold / distributed
- IL, NE
Why it was recalled
DAP chamber may be missing an insulating foil
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Cios Alpha VA20/ VA30 mobile X-Ray systems
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