Philips North America recalls
Philips North America appears in 563 official U.S. recall notices indexed by RecallRadar, most recently on 2026-10-07.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
- Ingenia 3.0T and 3.0T CX
FDA Device · Class II · 2026-10-07 · Philips North America - MR 7700
FDA Device · Class II · 2026-10-07 · Philips North America - SmartPath to MR 7700
FDA Device · Class II · 2026-10-07 · Philips North America - Upgrade to MR 7700
FDA Device · Class II · 2026-10-07 · Philips North America - Upgrade dStream
FDA Device · Class II · 2026-10-07 · Philips North America - MR 5300
FDA Device · Class II · 2026-10-07 · Philips North America - Ingenia 1.5T, 1.5T CX, and 1.5T S
FDA Device · Class II · 2026-10-07 · Philips North America - Ingenia Elition S and Ingenia Elition X
FDA Device · Class II · 2026-10-07 · Philips North America - Philips Medical Systems Technologies Ltd
FDA Device · Class II · 2026-10-07 · Philips North America - Ingenia Ambition S and Ingenia Ambition X
FDA Device · Class II · 2026-10-07 · Philips North America - Evolution upgrade 1.5T amd Evolution upgrade 3.0T
FDA Device · Class II · 2026-10-07 · Philips North America - SmartPath to dStream for 1.5T, SmartPath to dStream for 3.0T, SmartPath to dStream for XR and 3.0T, and SmartPath to Ingenia Elition X
FDA Device · Class II · 2026-10-07 · Philips North America - Ingenia Blue Seal SE and Blue Seal XE
FDA Device · Class II · 2026-10-07 · Philips North America - SmartPath to dStream for 1.5T, SmartPath to dStream for 3.0T, SmartPath to dStream for XR and 3.0T, SmartPath to Ingenia Elition X
FDA Device · Class II · 2026-09-30 · Philips North America - MR 7700 and Upgrade to MR 7700
FDA Device · Class II · 2026-09-30 · Philips North America - Ingenia 3.0T and Ingenia 3.0T CX
FDA Device · Class II · 2026-09-30 · Philips North America - Ingenia Elition S and Ingenia Elition X
FDA Device · Class II · 2026-09-30 · Philips North America - Name (Model Number): 1. Intera 1.5T (781195), 2. Intera 1.5T (781295), 3. Intera 1.5T Achieva IT Nova (781175), 4. Intera 1.5T Achieva Nova…
FDA Device · Class II · 2026-09-30 · Philips North America - Achieva 3.0T
FDA Device · Class II · 2026-09-30 · Philips North America - Evolution upgrade 1.5T and Evolution upgrade 3.0T
FDA Device · Class II · 2026-09-30 · Philips North America - Achieva XR
FDA Device · Class II · 2026-09-30 · Philips North America - Ingenia 1.5T, Ingenia 1.5T CX and Ingenia 1.5T S
FDA Device · Class II · 2026-09-30 · Philips North America - Achieva 1.5T, Achieva 1.5T Conversion and Achieva 1.5T Initial system
FDA Device · Class II · 2026-09-30 · Philips North America - MR 5300 Model Number (REF): 1. 782110, 2. 782152
FDA Device · Class II · 2026-09-30 · Philips North America - Ingenia Ambition S and Ingenia Ambition X
FDA Device · Class II · 2026-09-30 · Philips North America - Philips PIC iX Essentials REF:867093
FDA Device · Class II · 2026-09-23 · Philips North America - Philips Patient Information Center iX REF:866389
FDA Device · Class II · 2026-09-23 · Philips North America - Philips Brilliance
FDA Device · Class II · 2026-09-09 · Philips North America - Philips Ingenuity CT Product Codes: Ingenuity CT Upgrades 728327, Ingenuity CT China 728324, Ingenuity Core 128 Elite Brazil 728325
FDA Device · Class II · 2026-09-09 · Philips North America - Philips Brilliance CT 64: Brilliance CT 64 Channel Product Code: 728231, Brilliance CT 64 Upgrades Product Code: 728232
FDA Device · Class II · 2026-09-09 · Philips North America - Philips IQon Spectral CT Product Codes: IQon Spectral CT 728332, IQon Spectral CT 728331 Software 4.7.7.x
FDA Device · Class II · 2026-09-09 · Philips North America - Cardiac Workstation 7000
FDA Device · Class II · 2026-08-26 · Philips North America - Cardiac Workstation 5000
FDA Device · Class II · 2026-08-26 · Philips North America - Philips Avalon Fetal Monitor, FM 30 Part numberM2703A
FDA Device · Class II · 2026-07-01 · Philips North America - Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232
FDA Device · Class II · 2026-07-01 · Philips North America - Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703A
FDA Device · Class II · 2026-07-01 · Philips North America - DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035
FDA Device · Class II · 2026-06-17 · Philips North America - Philips Achieva 1.5T Initial system with MR Elastography (MRE). 1. Model Number (REF): 781178
FDA Device · Class II · 2026-05-06 · Philips North America - Philips Achieva 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781196. 2. Model Number (REF): 781296
FDA Device · Class II · 2026-05-06 · Philips North America - Philips SmartPath to dStream for 3.0T with MR Elastography (MRE). 1. Model Number (REF): 782145
FDA Device · Class II · 2026-05-06 · Philips North America - Philips Ingenia 1.5T CX with MR Elastography (MRE). 1. Model Number (REF): 781262
FDA Device · Class II · 2026-05-06 · Philips North America - Philips Ingenia Ambition S with MR Elastography (MRE). 1. Model Number (REF): 781359. 2. Model Number (REF): 782108. 3. Model Number (REF):…
FDA Device · Class II · 2026-05-06 · Philips North America - Philips Ingenia Ambition X with MR Elastography (MRE). 1. Model Number (REF): 781356. 2. Model Number (REF): 782109. 3. Model Number (REF):…
FDA Device · Class II · 2026-05-06 · Philips North America - Philips Evolution upgrade 3.0T with MR Elastography (MRE). 1. Model Number (REF): 782143. 2. Model Number (REF): 782162
FDA Device · Class II · 2026-05-06 · Philips North America - Philips Ingenia 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781342. 2. Model Number (REF): 781377. 3. Model Number (REF): 78210…
FDA Device · Class II · 2026-05-06 · Philips North America - Philips SmartPath to Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF): 782118. 2. Model Number (REF): 782144. 3. Model N…
FDA Device · Class II · 2026-05-06 · Philips North America - Philips Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF): 781358. 2. Model Number (REF): 782107. 3. Model Number (REF):…
FDA Device · Class II · 2026-05-06 · Philips North America - Philips MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782120. 2. Model Number (REF): 782153
FDA Device · Class II · 2026-05-06 · Philips North America - Philips Ingenia 3.0T CX with MR Elastography (MRE). 1. Model Number (REF): 781271. 2. Model Number (REF): 782105. 510(k) Numbers: K173079,…
FDA Device · Class II · 2026-05-06 · Philips North America - Philips SmartPath to dStream for XR and 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781270. 2. Model Number (REF): 782113
FDA Device · Class II · 2026-05-06 · Philips North America