Recall Z-3041-2026 ยท JAK System, X-Ray, Tomography, Computed
Philips North America Llc
Philips IQon Spectral CT Product Codes: IQon Spectral CT 728332, IQon Spectral CT 728331 Software 4.7.7.x
| Date | Sep 1, 2026 (initiated Aug 7, 2026) |
| Status | Open, Classified |
| Reason | 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. |
| Root cause | Radiation Control for Health and Safety Act |
| Action | Philips will inform customers of the issue via an Electronic Product Radiation Correction notification, dated "AUG 2026". Philips will schedule an appointment with remaining customers to update the software free of charge. Customers who need additional information or support concerning this issue should be directed to their local Philips representative at 1-800-722-9377 (Philips Customer Care Solutions Center). Philips reference: 2025-PD-CTAMI-014. |
| Distribution | US and US Territories. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K193454 | IQon Spectral CT Philips Medical Systems Nederland B.V., Jan 24, 2020 |