Siemens Medical Solutions USA, Inc recalls Artis Q and Q.Zen, Model Numbers:10848280, 10848281, 10848282, 10848353 & 10848355
- Recall date
- June 6, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0706-2018
- FDA classification
- Class II
- Brand / firm
- Siemens Medical Solutions USA, Inc
- Sold / distributed
- U.S. Nationwide
Why it was recalled
Potential for liquid entry
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Artis Q and Q.Zen, Model Numbers:10848280, 10848281, 10848282, 10848353 & 10848355
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