TemporaryFDAOngoing
Can cause harm that is usually temporary.
IQon Spectral CT IQon Spectral CT Upgrades
Check the device or its packaging for
FCO72800812; FCO72800814 728331 728332, DI (01)00884838059542
- Why
- The clinical CT scan may not automatically trigger after the Bolus Tracking scan and may need to be triggered manually. Additional Bolus Tracking shots may occur. This may result in the clinical acquisition being inadequate for diagnosis, causing a potential for patient rescan and receiving additional radiation.
- Distributed
- US Nationwide Distribution including Puerto Rico
- Company
- PHILIPS MEDICAL SYSTEMS
- Announced
- This is the date the recall was announced. A company may have started it weeks earlier.
- Recall began
Source: FDA record Z-2651-2026 · retrieved 27 July 2026
Read the official notice