Philips North America Llc: Philips Brilliance. Models: Brilliance Ict, Brilliance Ict Upgrades, Brilliance Ict Sp. Software 4.1.10.x Product Codes: 728306, 728305, 728311
- Recalling firm
- Philips North America Llc
- Product
- Philips Brilliance. Models: Brilliance iCT, Brilliance iCT Upgrades, Brilliance iCT SP. Software 4.1.10.x Product Codes: 728306, 728305, 728311.
- 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
- Category
- medical device recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-08-07
- Status
- Ongoing
- Distribution
- US and US Territories.
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/f6496e36-5e2b-4667-86f6-f8f1702193d0