IQon Spectral CT IQon Spectral CT Upgrades recall
IQon Spectral CT IQon Spectral CT Upgrades
Why was IQon Spectral CT IQon Spectral CT Upgrades 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 should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
FCO72800812; FCO72800814 728331 728332, DI (01)00884838059542
- Product
- IQon Spectral CT IQon Spectral CT Upgrades
- Recalling firm
- PHILIPS MEDICAL SYSTEMS
- Quantity
- 42
- Distribution
- US Nationwide Distribution including Puerto Rico
- Recall date
- August 5, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)