Philips Medical Systems: System, X-ray, Tomography, Computed
Recall Summary Philips is recalling several models of CT scanning machines because the automatic trigger for clinical scans may fail after a Bolus Tracking scan, requiring manual activation. This malfunction can result in inadequate scan images that may require patients to undergo repeat scans and receive additional radiation exposure. The recall affects Philips CT equipment distributed nationwide across the United States and Puerto Rico.
- Recalling firm
- PHILIPS MEDICAL SYSTEMS
- Product
- Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP Brilliance CT 64 Channel CT6000 Brilliance 64 Upgrades
- Reason
- 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.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-06-11
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide Distribution including Puerto Rico
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/22daaa34-3743-4f8f-ab4f-f44f29ccb055