Philips North America Llc: Philips Iqon Spectral Ct Product Codes: Iqon Spectral Ct 728332, Iqon Spectral Ct 728331 Software 4.7.7.x

Recalling firm
Philips North America Llc
Product
Philips IQon Spectral CT Product Codes: IQon Spectral CT 728332, IQon Spectral CT 728331 Software 4.7.7.x
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.
Classification
Class II
Category
medical device recall
Country
United States
Agency
U.S. Food and Drug Administration
Recall date
2026-08-07
Status
Ongoing
Distribution
US and US Territories.

Official recall notice from U.S. Food and Drug Administration

Recall details on Nibble Recalls: https://trynibble.app/recalls/272c6527-86b0-4b67-9597-03dda368571b