Recall Z-2650-2026
- Recall number
- Z-2650-2026
- Event number
- 99352
- Firm
- PHILIPS MEDICAL SYSTEMS
- Firm FEI
- 3017726341
- Product code
- JAK
- Status
- Open, Classified
- Initiated
- 2026-06-11
- Posted
- 2026-07-27
- Root cause
- Radiation Control for Health and Safety Act
- 510(k) numbers
- K250648, K993645, K253173, K233767, K242874, K023785, K171677, K151833, K102102, K212875, K181646, K090220, K082458, K790395, K861708, K032243, K944326, K203187, K233753, K153004, K182716, K232412, K073138, K780115, K052587, K010817, K911764, K232227, K201586, K142955
Product#
Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP Brilliance CT 64 Channel CT6000 Brilliance 64 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.