Philips North America recalls

Philips North America has 531 recalls on record with the FDA and USDA, the earliest in 2017 and the latest reported on 9 Sep 2026. 424 are still ongoing. 85 were reported in the last 12 months.

Total recalls531since 2017

Last 12 months85reported

Class I92% of total

Ongoing424latest 9 Sep 2026

Recalls per month, last 24 months

click a bar for that month

18Oct '24 0 15 0Jan '25 5 0 6Apr 19 9 1Jul 19 0 12Oct 0 25 2Jan '26 17 0 0Apr 19 1 3Jul 2 4

Severity split

Class I 9 2%Class II 514 97%Class III 8 2%

Why philips north america is recalled

Product types

By year

2026489%
20259618%
202415930%
20235811%
2022224%
20216412%
2020479%
2019346%
201820%
201710%

Ongoing philips north america recalls

424 active

Reported	Class	Recall	Company	Reason	Where
9 Sep 2026Device	CLASS II	Philips Brilliance recalled by Philips North America	Philips North America	Device Malfunction	MA
9 Sep 2026Device	CLASS II	Philips IQon Spectral CT Product Codes recalled by Philips North America	Philips North America	Device Malfunction	MA
9 Sep 2026Device	CLASS II	Philips Ingenuity CT Product Codes recalled by Philips North America	Philips North America	Device Malfunction	MA
9 Sep 2026Device	CLASS II	Philips Brilliance CT 64: Brilliance CT 64 Channel Product recalled	Philips North America	Device Malfunction	MA
26 Aug 2026Device	CLASS II	Cardiac Workstation recalled by Philips North America	Philips North America	Labeling Errors	Nationwide
26 Aug 2026Device	CLASS II	Cardiac Workstation recalled by Philips North America	Philips North America	Labeling Errors	Nationwide

All philips north america recalls, newest first

531 total

Reported	Class	Recall	Company	Reason	Where
9 Sep 2026Device	CLASS II	Philips Brilliance recalled by Philips North America	Philips North America	Device Malfunction	MA
9 Sep 2026Device	CLASS II	Philips IQon Spectral CT Product Codes recalled by Philips North America	Philips North America	Device Malfunction	MA
9 Sep 2026Device	CLASS II	Philips Ingenuity CT Product Codes recalled by Philips North America	Philips North America	Device Malfunction	MA
9 Sep 2026Device	CLASS II	Philips Brilliance CT 64: Brilliance CT 64 Channel Product recalled	Philips North America	Device Malfunction	MA
26 Aug 2026Device	CLASS II	Cardiac Workstation recalled by Philips North America	Philips North America	Labeling Errors	Nationwide
26 Aug 2026Device	CLASS II	Cardiac Workstation recalled by Philips North America	Philips North America	Labeling Errors	Nationwide
1 Jul 2026Device	CLASS II	Philips Telemetry Monitor 5500 4 GHz recalled by Philips North America	Philips North America	Lead & Heavy Metals	Nationwide
1 Jul 2026Device	CLASS II	Philips Avalon Fetal Monitor, FM 30 Part numberM2703A recalled	Philips North America	Other	Nationwide
1 Jul 2026Device	CLASS II	Philips Avalon Fetal Monitor, FM20 recalled by Philips North America	Philips North America	Other	Nationwide
17 Jun 2026Device	CLASS II	DigitalDiagnost C90 Flex/Value/Chest/ER recalled	Philips North America	Potency & Assay	CA

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.