Philips Medical Systems recalls

Philips Medical Systems has 81 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 5 Aug 2026. 11 are still ongoing. 7 were reported in the last 12 months. The most frequent reason is device malfunction.

Total recalls81since 2013

Last 12 months7reported

Class I11% of total

Ongoing11latest 5 Aug 2026

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 3Nov 0 0 0Feb 0 1 0May 0 0 3Aug 0 0

Severity split

Class I 1 1%Class II 80 99%Class III 0 0%

Why philips medical systems is recalled

Product types

By year

202645%
202534%
202445%
201679%
20152733%
20143543%
201311%

Ongoing philips medical systems recalls

11 active

Reported	Class	Recall	Company	Reason	Where
5 Aug 2026Device	CLASS II	Ingenuity CT CT5000 Ingenuity Plus CT5000 Ingenuity Pro recalled	Philips Medical Systems	Device Malfunction	Nationwide
5 Aug 2026Device	CLASS II	Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP recalled	Philips Medical Systems	Device Malfunction	Nationwide
5 Aug 2026Device	CLASS II	IQon Spectral CT IQon Spectral CT Upgrades recalled	Philips Medical Systems	Device Malfunction	Nationwide
22 Apr 2026Device	CLASS II	Philips Spectral CT on Rails recalled by Philips Medical Systems	Philips Medical Systems	Device Malfunction	Nationwide
5 Nov 2025Device	CLASS II	Model: Incisive CT; Product Code (REF): (1) 728143, (2) recalled	Philips Medical Systems	Device Malfunction	18 states
5 Nov 2025Device	CLASS II	Model: CT 5300; Product Code (REF): 728285; Software Versions recalled	Philips Medical Systems	Device Malfunction	18 states

All philips medical systems recalls, newest first

81 total

Reported	Class	Recall	Company	Reason	Where
5 Aug 2026Device	CLASS II	Ingenuity CT CT5000 Ingenuity Plus CT5000 Ingenuity Pro recalled	Philips Medical Systems	Device Malfunction	Nationwide
5 Aug 2026Device	CLASS II	Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP recalled	Philips Medical Systems	Device Malfunction	Nationwide
5 Aug 2026Device	CLASS II	IQon Spectral CT IQon Spectral CT Upgrades recalled	Philips Medical Systems	Device Malfunction	Nationwide
22 Apr 2026Device	CLASS II	Philips Spectral CT on Rails recalled by Philips Medical Systems	Philips Medical Systems	Device Malfunction	Nationwide
5 Nov 2025Device	CLASS II	Model: Incisive CT; Product Code (REF): (1) 728143, (2) recalled	Philips Medical Systems	Device Malfunction	18 states
5 Nov 2025Device	CLASS II	Model: CT 5300; Product Code (REF): 728285; Software Versions recalled	Philips Medical Systems	Device Malfunction	18 states
5 Nov 2025Device	CLASS II	Model: Incisive CT for Brazil SKD; Product Code (REF) recalled	Philips Medical Systems	Device Malfunction	18 states
21 Feb 2024Device	CLASS II	CombiDiagnost R90 1.0 (709030) recalled by Philips Medical Systems	Philips Medical Systems	Other	Nationwide
21 Feb 2024Device	CLASS II	CombiDiagnost R90 1.1 (709031) recalled by Philips Medical Systems	Philips Medical Systems	Other	Nationwide
14 Feb 2024Device	CLASS II	Spectral CT on Rails recalled by Philips Medical Systems	Philips Medical Systems	Labeling Errors	Nationwide
14 Feb 2024Device	CLASS II	Spectral CT recalled by Philips Medical Systems	Philips Medical Systems	Labeling Errors	Nationwide
12 Oct 2016Device	CLASS II	Ingenuity Core recalled by Philips Medical Systems	Philips Medical Systems	Other	Nationwide
12 Oct 2016Device	CLASS II	Brilliance 64 CT Model Number 728231 Product Usage: Computed recalled	Philips Medical Systems	Other	Nationwide
12 Oct 2016Device	CLASS II	Ingenuity CT recalled by Philips Medical Systems	Philips Medical Systems	Other	Nationwide
12 Oct 2016Device	CLASS II	Ingenuity Core recalled by Philips Medical Systems	Philips Medical Systems	Other	Nationwide
6 Apr 2016Device	CLASS II	Foot Switches used with the following systems recalled	Philips Medical Systems	Other	Nationwide
6 Apr 2016Device	CLASS II	Foot Switches used with Philips MultiDiagnost Eleva recalled	Philips Medical Systems	Other	Nationwide
10 Feb 2016Device	CLASS II	DS/US Proton Feature with Pinnacle3 recalled by Philips Medical Systems	Philips Medical Systems	Device Malfunction	Nationwide
16 Dec 2015Device	CLASS II	Philips IntelliVue Information Center iX (release A.00 recalled	Philips Medical Systems	Device Malfunction	Nationwide
9 Dec 2015Device	CLASS II	Philips Healthcare Allure BiPlane Series recalled	Philips Medical Systems	Other	Nationwide
9 Dec 2015Device	CLASS II	Philips Healthcare Xper cardio systems recalled	Philips Medical Systems	Other	Nationwide
9 Dec 2015Device	CLASS II	Philips Healthcare Xper cardio systems R7.6 recalled	Philips Medical Systems	Other	Nationwide
9 Dec 2015Device	CLASS II	Philips Healthcare Xper vascular system recalled	Philips Medical Systems	Other	Nationwide
9 Dec 2015Device	CLASS II	Patient Support Material Number recalled by Philips Medical Systems	Philips Medical Systems	Device Malfunction	11 states
9 Dec 2015Device	CLASS II	Patient Support Material Number: 9890 010 87431 used recalled	Philips Medical Systems	Device Malfunction	11 states
9 Dec 2015Device	CLASS II	Philips Healthcare Integris cardio system recalled	Philips Medical Systems	Other	Nationwide
9 Dec 2015Device	CLASS II	Philips Healthcare Allura Xper Series recalled	Philips Medical Systems	Other	Nationwide
9 Dec 2015Device	CLASS II	Philips Healthcare Integris H5000F/Allura 9F recalled	Philips Medical Systems	Other	Nationwide
9 Dec 2015Device	CLASS II	Philips Healthcare Xper vascular systems R7.6 recalled	Philips Medical Systems	Other	Nationwide
9 Dec 2015Device	CLASS II	Philips Healthcare Integris vascular System recalled	Philips Medical Systems	Other	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.