Philips North America recalls

Philips North America has 558 recalls on record with the FDA and USDA, the earliest in 2017 and the latest reported on 7 Oct 2026. 451 are still ongoing. 102 were reported in the last 12 months.

Total recalls558since 2017

Last 12 months102reported

Class I92% of total

Ongoing451latest 7 Oct 2026

Recalls per month, last 24 months

click a bar for that month

0Nov '24 15 0 5Feb 0 6 19May 9 1 19Aug 0 12 0Nov 25 2 17Feb 0 0 19May 1 3 2Aug 18 13

Severity split

Class I 9 2%Class II 541 97%Class III 8 1%

Why philips north america is recalled

Product types

By year

20267513%
20259617%
202415928%
20235810%
2022224%
20216411%
2020478%
2019346%
201820%
201710%

Ongoing philips north america recalls

451 active

Reported	Class	Recall	Company	Reason	Where
7 Oct 2026Device	CLASS II	SmartPath to dStream for XR and 3.0T recalled by Philips North America	Philips North America	Device Malfunction	Nationwide
7 Oct 2026Device	CLASS II	Upgrade to MR recalled by Philips North America	Philips North America	Device Malfunction	Nationwide
7 Oct 2026Device	CLASS II	Ingenia Elition S and Ingenia Elition recalled by Philips North America	Philips North America	Device Malfunction	Nationwide
7 Oct 2026Device	CLASS II	Ingenia Ambition S and Ingenia Ambition recalled	Philips North America	Device Malfunction	Nationwide
7 Oct 2026Device	CLASS II	Ingenia Blue Seal SE and Blue Seal XE recalled by Philips North America	Philips North America	Device Malfunction	Nationwide
7 Oct 2026Device	CLASS II	SmartPath to MR recalled by Philips North America	Philips North America	Device Malfunction	Nationwide

All philips north america recalls, newest first

558 total

Reported	Class	Recall	Company	Reason	Where
7 Oct 2026Device	CLASS II	SmartPath to dStream for XR and 3.0T recalled by Philips North America	Philips North America	Device Malfunction	Nationwide
7 Oct 2026Device	CLASS II	Upgrade to MR recalled by Philips North America	Philips North America	Device Malfunction	Nationwide
7 Oct 2026Device	CLASS II	Ingenia Elition S and Ingenia Elition recalled by Philips North America	Philips North America	Device Malfunction	Nationwide
7 Oct 2026Device	CLASS II	Ingenia Ambition S and Ingenia Ambition recalled	Philips North America	Device Malfunction	Nationwide
7 Oct 2026Device	CLASS II	Ingenia Blue Seal SE and Blue Seal XE recalled by Philips North America	Philips North America	Device Malfunction	Nationwide
7 Oct 2026Device	CLASS II	SmartPath to MR recalled by Philips North America	Philips North America	Device Malfunction	Nationwide
7 Oct 2026Device	CLASS II	MR 5300; Model number (REF): 1. 782110, 2. 782152 recalled	Philips North America	Device Malfunction	Nationwide
7 Oct 2026Device	CLASS II	Upgrade dStream recalled by Philips North America	Philips North America	Device Malfunction	Nationwide
7 Oct 2026Device	CLASS II	Philips Medical Systems Technologies Ltd recalled	Philips North America	Device Malfunction	MA
7 Oct 2026Device	CLASS II	Evolution upgrade 1.5T amd Evolution upgrade 3.0T recalled	Philips North America	Device Malfunction	Nationwide
7 Oct 2026Device	CLASS II	Ingenia 1.5T, 1.5T CX, and 1.5T recalled by Philips North America	Philips North America	Device Malfunction	Nationwide
7 Oct 2026Device	CLASS II	MR 7700; Model number (REF): 1. 782120, 2. 782153 recalled	Philips North America	Device Malfunction	Nationwide
7 Oct 2026Device	CLASS II	Ingenia 3.0T and 3.0T CX recalled by Philips North America	Philips North America	Device Malfunction	Nationwide
30 Sep 2026Device	CLASS II	SmartPath to dStream for XR and 3.0T recalled by Philips North America	Philips North America	Device Malfunction	Nationwide
30 Sep 2026Device	CLASS II	Achieva 1.5T, Achieva 1.5T Conversion recalled by Philips North America	Philips North America	Device Malfunction	Nationwide
30 Sep 2026Device	CLASS II	Ingenia Ambition S and Ingenia Ambition recalled	Philips North America	Device Malfunction	Nationwide
30 Sep 2026Device	CLASS II	Name (Model Number): 1. Intera 1.5T (781195), 2. Intera 1.5T recalled	Philips North America	Device Malfunction	Nationwide
30 Sep 2026Device	CLASS II	Ingenia 3.0T and Ingenia 3.0T CX recalled by Philips North America	Philips North America	Device Malfunction	Nationwide
30 Sep 2026Device	CLASS II	Evolution upgrade 1.5T and Evolution upgrade 3.0T recalled	Philips North America	Device Malfunction	Nationwide
30 Sep 2026Device	CLASS II	Achieva XR recalled by Philips North America	Philips North America	Device Malfunction	Nationwide
30 Sep 2026Device	CLASS II	Ingenia 1.5T, Ingenia 1.5T CX and Ingenia 1.5T recalled	Philips North America	Device Malfunction	Nationwide
30 Sep 2026Device	CLASS II	MR 5300 Model Number (REF): 1. recalled by Philips North America	Philips North America	Device Malfunction	Nationwide
30 Sep 2026Device	CLASS II	MR 7700 and Upgrade to MR recalled by Philips North America	Philips North America	Device Malfunction	Nationwide
30 Sep 2026Device	CLASS II	Ingenia Elition S and Ingenia Elition recalled by Philips North America	Philips North America	Device Malfunction	Nationwide
30 Sep 2026Device	CLASS II	Achieva 3.0T recalled by Philips North America	Philips North America	Device Malfunction	Nationwide
23 Sep 2026Device	CLASS II	Philips Patient Information Center iX recalled by Philips North America	Philips North America	Device Malfunction	Nationwide
23 Sep 2026Device	CLASS II	Philips PIC iX Essentials recalled by Philips North America	Philips North America	Device Malfunction	Nationwide
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 recalled by Philips North America	Philips North America	Device Malfunction	MA
9 Sep 2026Device	CLASS II	Philips Ingenuity CT recalled by Philips North America	Philips North America	Device Malfunction	MA

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.