Recall
FDAHealthJune 11, 2026

PHILIPS MEDICAL SYSTEMS — IQon Spectral CT IQon Spectral CT Upgrades

⚠️ 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.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
June 11, 2026

US Nationwide Distribution including Puerto Rico

What's affected?

Product
IQon Spectral CT IQon Spectral CT Upgrades
Lot code
FCO72800812; FCO72800814 728331 728332, DI (01)00884838059542

Additional details

FCO72800812; FCO72800814 728331 728332, DI (01)00884838059542

What should I do?

Recommended action

Class II recall. FDA Mandated Quantity affected: 42.

View original FDA notice →

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