Brand

PHILIPS MEDICAL SYSTEMS: official recall notices

7 official recall or safety notices on this site name PHILIPS MEDICAL SYSTEMS, dated between 2025-09-25 and 2026-06-11. They were issued by 1 authority: US FDA — Medical Devices (7).

Countries where the notices were issued: United States (7).

Name as written in the notices: PHILIPS MEDICAL SYSTEMS. This is the brand or the responsible company as each authority recorded it. A recall shows a safety system working; it is not a verdict on a brand. Follow the official notice for each product.

Notices by year

Year	Notices
2026	4
2025	3

Notices by authority

Authority	Notices
US FDA — Medical Devices	7

All notices

Date	Authority	Product	Hazard (as classified)
2026-06-11	US FDA — Medical Devices	IQon Spectral CT IQon Spectral CT Upgrades	—
2026-06-11	US FDA — Medical Devices	Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP Brilliance CT 64 Channel CT6000 Brilliance 64 Upgrades	—
2026-06-11	US FDA — Medical Devices	Ingenuity CT CT5000 Ingenuity Plus CT5000 Ingenuity Pro CT5000 Ingenuity Premium Ingenuity CT Upgrades Ingenuity CT	—
2026-03-07	US FDA — Medical Devices	Philips Spectral CT on Rails. Model Number: 728334.	—
2025-09-25	US FDA — Medical Devices	Model: Incisive CT for Brazil SKD; Product Code (REF): 728146; Software Versions: 5.1.0.X & 5.1.1.X;	—
2025-09-25	US FDA — Medical Devices	Model: CT 5300; Product Code (REF): 728285; Software Versions: 5.1.0.X & 5.1.1.X;	—
2025-09-25	US FDA — Medical Devices	Model: Incisive CT; Product Code (REF): (1) 728143, (2) 728144; Software Versions: 5.1.0.X & 5.1.1.X;	—

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