Class II

Medical Device Recall: Artis Pheno. Image-Intensified Flouroscopic X-Ray System.

Siemens Medical Solutions USA, Inc · August 12, 2025

Reason for Recall

Limited system movements after startup .

Distribution

US Nationwide distribution in the states of AL, AZ, FL, KY, MA, MI, NY, OR, A, TN, TX & UT.

States Affected

NATIONWIDE

Quantity Affected

20 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2529-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Siemens Medical Solutions USA, Inc Medical Device Recall: Artis Pheno. Image-Intensified Flouroscopic X-Ray System. | SafeCheck