Philips North America Llc: System, X-ray, Tomography, Computed
- Recalling firm
- 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
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-08-07
- Status
- Open, Classified
- Distribution
- US and US Territories.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/a1dfd697-8520-4250-86aa-6fa1475f11d3