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Medical Device

IQon Spectral CT IQon Spectral CT Upgrades

Recall date: 2026-08-05 · Source: FDA_DEVICE
Brand / Firm
PHILIPS MEDICAL SYSTEMS
Product
IQon Spectral CT IQon Spectral CT Upgrades
Reason for recall
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.
Units affected
42
Description
IQon Spectral CT IQon Spectral CT Upgrades
View official recall notice →