Siemens Medical Solutions USA, Inc recalls ARTIS Pheno VE30A and VE40A
- Recalling company
- Siemens Medical Solutions USA, Inc
- Product
- ARTIS Pheno VE30A and VE40A, Model 10849000
- Reason
- 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.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Mar 12, 2026
- Reported
- Apr 22, 2026
- Distribution
- U.S. and O.U.S.
- Status
- Ongoing
- Quantity
- 73
- Lot / codes
- UDI 04056869046877
- Company location
- Malvern, PA
- Recall type
- FDA Mandated
- Recall number
- Z-1814-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1814-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.