Philips North America recalls

Philips North America has 545 recalls on record with the FDA and USDA, the earliest in 2017 and the latest reported on 30 Sep 2026. 438 are still ongoing. 89 were reported in the last 12 months.

Total recalls545since 2017

Last 12 months89reported

Class I92% of total

Ongoing438latest 30 Sep 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 0

Severity split

Class I 9 2%Class II 528 97%Class III 8 1%

Why philips north america is recalled

Product types

By year

20266211%
20259618%
202415929%
20235811%
2022224%
20216412%
2020479%
2019346%
201820%
201710%

Ongoing philips north america recalls

438 active

Reported	Class	Recall	Company	Reason	Where
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

All philips north america recalls, newest first

545 total

Reported	Class	Recall	Company	Reason	Where
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
9 Sep 2026Device	CLASS II	Philips Brilliance CT 64: Brilliance CT 64 Channel 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 1.4 GHz recalled by Philips North America	Philips North America	Device Malfunction	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
6 May 2026Device	CLASS II	Philips SmartPath to dStream for 1.5T with MR Elastography (MRE) recalled	Philips North America	Other	Nationwide
6 May 2026Device	CLASS II	Philips SmartPath to dStream for XR and 3.0T recalled	Philips North America	Other	Nationwide
6 May 2026Device	CLASS II	Philips Ingenia Ambition X with MR Elastography (MRE) recalled	Philips North America	Other	Nationwide
6 May 2026Device	CLASS II	Philips Upgrade to MR 7700 with MR Elastography (MRE) recalled	Philips North America	Other	Nationwide
6 May 2026Device	CLASS II	Philips Ingenia Elition S with MR Elastography (MRE) recalled	Philips North America	Other	Nationwide
6 May 2026Device	CLASS II	Philips Evolution Upgrade 1.5T with MR Elastography (MRE) recalled	Philips North America	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.