Philips North America Llc recalls Philips IQon Spectral CT Product Codes: IQon Spectral CT 728332
- Recalling company
- Philips North America Llc
- Product
- Philips IQon Spectral CT Product Codes: IQon Spectral CT 728332, IQon Spectral CT 728331 Software 4.7.7.x
- Reason
- Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the equipment.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Aug 7, 2026
- Reported
- Sep 9, 2026
- Distribution
- US and US Territories.
- Status
- Ongoing
- Quantity
- N/A
- Lot / codes
- UDI:N/A
- Company location
- Cambridge, MA
- Recall type
- FDA Mandated
- Recall number
- Z-3041-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-3041-2026 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.