Class II

Medical Device Recall: Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP Brilliance CT 64 Channel CT6000 Brilliance 64 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

128

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2650-2026

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.