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Can cause harm that is usually temporary.

Philips IQon Spectral CT Product Codes: IQon Spectral CT 728332, IQon Spectral CT 728331 Software 4.7.7.x

Check the device or its packaging for

UDI:N/A

Why: 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.
Distributed: US and US Territories.
Company: Philips North America Llc
Announced: 9 September 2026This is the date the recall was announced. A company may have started it weeks earlier.
Recall began: 7 August 2026

Source: FDA record Z-3041-2026 · retrieved 1 September 2026

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