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PHILIPS MEDICAL SYSTEMS recalls Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP Brilliance CT 64 Channel CT6000 Brilliance 64 Upgrades
Recalled August 5, 2026 · FDA recall Z-2650-2026 · PHILIPS MEDICAL SYSTEMS
Hazard
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. · FDA Class II
Units
128
Sold at
US Nationwide Distribution including Puerto Rico
Description
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.
Product
Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP Brilliance CT 64 Channel CT6000 Brilliance 64 Upgrades
Manufacturer(s)
PHILIPS MEDICAL SYSTEMS
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →