Siemens Medical Solutions USA, Inc recalls Artis Pheno. Image-Intensified Flouroscopic X-Ray System.
- Recall date
- August 12, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2529-2025
- FDA classification
- Class II
- Brand / firm
- Siemens Medical Solutions USA, Inc
- Sold / distributed
- US Nationwide distribution in the states of AL, AZ, FL, KY, MA, MI, NY, OR, A, TN, TX & UT.
Why it was recalled
Limited system movements after startup .
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 Pheno. Image-Intensified Flouroscopic X-Ray System.
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