IQon Spectral CT IQon Spectral CT Upgrades recall
PHILIPS MEDICAL SYSTEMS recalled IQon Spectral CT IQon Spectral CT Upgrades on August 5, 2026 because of the clinical CT scan may not automatically trigger after the Bolus Tracking scan and may need to be triggered manually. It was sold nationwide.
Why it was recalled
The clinical CT scan may not automatically trigger after the Bolus Tracking scan and may need to be triggered manually. Additional Bolus Tracking shots may occur. This may result in the clinical acquisition being inadequate for diagnosis, causing a potential for patient rescan and receiving additional radiation.
What's recalled
IQon Spectral CT IQon Spectral CT Upgrades
Quantity: 42
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 MEDICAL SYSTEMS, Cambridge, MA
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
US Nationwide Distribution including Puerto Rico - Status
- Ongoing
- Recall number
- Z-2651-2026
- Source
- U.S. Food and Drug Administration
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