PHILIPS MEDICAL SYSTEMS recalls 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…
Read the official notice →- Date
- 2026-08-05
- Country
- United States
- Brand
- Philips Medical Systems
- Product
- IQon Spectral CT IQon Spectral CT Upgrades
- Classification
- Class II
- Units
- US Nationwide Distribution including Puerto Rico
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
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- Check the product name, strength and lot number against the official notice.
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General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
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