Philips North America Llc recalls Philips Brilliance CT 64: Brilliance CT 64 Channel Product Code: 728231
- Recalling company
- Philips North America Llc
- Product
- Philips Brilliance CT 64: Brilliance CT 64 Channel Product Code: 728231, Brilliance CT 64 Upgrades Product Code: 728232. Software 4.1.10.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
- Brilliance CT 64 Channel UDI (01)00884838083325. Brilliance CT 64 Upgrades UDI N/A.
- Company location
- Cambridge, MA
- Recall type
- FDA Mandated
- Recall number
- Z-3043-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-3043-2026 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.