Class II
Medical Device Recall: Philips Ingenuity CT Product Codes: Ingenuity CT Upgrades 728327, Ingenuity CT China 728324, Ingenuity Core 128 Elite Brazil 728325. Software 4.4.10.x
Philips North America Llc · August 7, 2026
Reason for Recall
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.
Distribution
US and US Territories.
Quantity Affected
N/A
Source: FDA (openFDA Device Enforcement)
Recall number: Z-3042-2026
Status: ongoing
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