Siemens Medical Solutions USA, Inc recalls CIOS ALPHA; image intensified fluoroscopic x-ray system
- Recall date
- August 17, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0118-2016
- FDA classification
- Class II
- Brand / firm
- Siemens Medical Solutions USA, Inc
- Sold / distributed
- Nationwide Distribution.
Why it was recalled
patient procedure interruption due to a potential system failure
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; image intensified fluoroscopic x-ray system
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