FDA Medical devices recall ·
IQon Spectral CT IQon Spectral CT Upgrades recall
- Recall number
- Z-2651-2026
- Date
- (initiated June 11, 2026)
- Company / brand
- Philips Medical Systems
222 Jacobs St, Cambridge, MA, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 42
- Initiated by
- FDA Mandated
Read the official FDA notice ↗
Product
IQon Spectral CT IQon Spectral CT Upgrades
Why was it 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 you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
FCO72800812; FCO72800814 728331 728332, DI (01)00884838059542
Distribution
US Nationwide Distribution including Puerto Rico
States: Puerto Rico
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2651-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.