Class II
Medical Device Recall: IQon Spectral CT IQon Spectral CT Upgrades
PHILIPS MEDICAL SYSTEMS · June 11, 2026
Reason for Recall
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.
Distribution
US Nationwide Distribution including Puerto Rico
States Affected
NATIONWIDE
Quantity Affected
42
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2651-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.