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.

Siemens Medical Solutions USA, Inc Medical Device Recall: ARTIS Pheno VE30A and VE40A, Model 10849000 | SafeCheck