FDAFDA · Food and drugs·Recall number Z-3041-2026
Philips IQon Spectral CT Product Codes: IQon Spectral CT 728332, IQon Spectral CT 728331 Software 4.7.7.x
Published September 9, 2026 · Recall initiated: August 7, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
FDA Mandated
Recall details
- Manufacturer
- Philips North America Llc
- Distributor
- US and US Territories.
- Lot
- UDI:N/A
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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