Device recalls

Philips Brilliance. Models: Brilliance iCT, Brilliance iCT Upgrades, Brilliance iCT SP. Software 4.1.10.x Product Codes: 728306, 728305, 72…

Philips North America Llc · Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of t…

Open, ClassifiedRadiation Control for Health and Safety ActZ-3040-2026
Open FDA's page for this record
Cfres ID
222477
Product res number
Z-3040-2026
Event date initiated
2026-08-07
Event date posted
2026-09-01
Recall status
Open, Classified
Res event number
99784
Product code
JAK
Product description
Philips Brilliance. Models: Brilliance iCT, Brilliance iCT Upgrades, Brilliance iCT SP. Software 4.1.10.x Product Codes: 728306, 728305, 728311.
Code info
UDI for Brilliance iCT: (01)00884838059474, UDI for Brilliance iCT Upgrades: N/A, UDI for Brilliance iCT SP: N/A.
Firm FEI number
3016618143
Recalling firm
Philips North America Llc
Address 1
222 Jacobs St
City
Cambridge
State
MA
Postal code
02141-2289
Root cause description
Radiation Control for Health and Safety Act
Distribution pattern
US and US Territories.
Reason for recall

Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the equipment.

Action

Philips will inform customers of the issue via an Electronic Product Radiation Correction notification, dated "AUG 2026". Philips will schedule an appointment with remaining customers to update the software free of charge. Customers who need additional information or support concerning this issue should be directed to their local Philips representative at 1-800-722-9377 (Philips Customer Care Solutions Center). Philips reference: 2025-PD-CTAMI-014.

K numbers
K250648
Harmonized identifiers (openFDA)
Device name
System, X-Ray, Tomography, Computed
Medical specialty description
Radiology
Regulation number
892.1750
Device class
2
K number
K213999, K910859, K193073, K063184, K093146, K123500, K090991, K792603, K160350, K033502, K982265, K964890, K120833, K974513, K222819, K884671, K871859, K991766, K812509, K132410, K761330, K151673, K241713, K072606, K142222, K884788, K232155, K942040, K153429, K183202, K073373, K120546, K173821, K240369, K803181, K133424, K974344, K161157, K013214, K894888 +784 more
Registration number
3017425975, 3004056159, 3008632256, 8022257, 3003678543, 3023003446, 3033527283, 3015223550, 3017210169, 9617978, 3027339477, 3001722928, 3013679558, 3019216, 3017426576, 1226188, 3003967489, 3023140882, 3012761544, 3006209933, 9611343, 3015777306, 3033527273, 2520313, 3002808157, 3042175844, 3008355361, 3004083736, 3010398867, 3012453401, 3039211310, 3005930550, 3042172882, 3012938564, 8043933, 3012044688, 3004753774, 3031503890, 3004977335, 3013035022 +126 more
FEI number
3004056159, 3008632256, 3003678543, 3023003446, 3033527283, 3015223550, 3017210169, 3002807880, 3001726808, 3027339477, 3001722928, 3013679558, 3019216, 3017426576, 3004571294, 3003967489, 1000139922, 3023140882, 3012761544, 3006209933, 3033527273, 3015777306, 2520313, 3002808157, 3008355361, 3004083736, 3010398867, 3012453401, 3039211310, 3002619595, 3005930550, 3042172882, 1000514697, 3012938564, 3003757840, 3012044688, 3004753774, 3031503890, 3002807903, 3004977335 +126 more
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.