Philips IQon Spectral CT Product Codes recall
Philips North America Llc recalled Philips IQon Spectral CT Product Codes on September 9, 2026 because of 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. It was sold in US and US Territories..
Why it was recalled
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's recalled
Philips IQon Spectral CT Product Codes: IQon Spectral CT 728332, IQon Spectral CT 728331 Software 4.7.7.x
Quantity: N/A
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Philips North America Llc, Cambridge, MA
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- US and US Territories.
- Status
- Ongoing
- Recall number
- Z-3041-2026
- Source
- U.S. Food and Drug Administration
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