Class II
Medical Device Recall: ARTIS Pheno VE30A and VE40A, Model 10849000
Siemens Medical Solutions USA, Inc · March 12, 2026
Reason for Recall
During 3D acquisitions, lighter and darker patient images may be captured, which may result in less accurate 3D reconstruction. The variation of brightness is a result of a constant unregulated medium dose and the angular change of patient diameter caused by rotational acquisition. This may result in unintentional low-dose radiation exposure to a patient.
Distribution
U.S. and O.U.S.
Quantity Affected
73
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1814-2026
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.