Siemens Medical Solutions USA, Inc recalls ARTISTE" MV System
- Recall date
- February 14, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1488-2017
- FDA classification
- Class II
- Brand / firm
- Siemens Medical Solutions USA, Inc
- Sold / distributed
- Distributed throughout the United States
Why it was recalled
Software update
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
ARTISTE" MV System
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