Philips North America recalls
Philips North America appears in 532 official U.S. recall notices indexed by RecallRadar, most recently on 2026-08-26.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
- 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 - Philips Achieva 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781278
FDA Device · Class II · 2026-05-06 · Philips North America - Philips Ingenia Elition S with MR Elastography (MRE). 1. Model Number (REF): 781357. 2. Model Number (REF): 782106. 3. Model Number (REF):…
FDA Device · Class II · 2026-05-06 · Philips North America - Philips Upgrade to MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782130
FDA Device · Class II · 2026-05-06 · Philips North America - Philips Ingenia 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781315. 2. Model Number (REF): 781341. 3. Model Number (REF): 78139…
FDA Device · Class II · 2026-05-06 · Philips North America - Philips SmartPath to dStream for 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781260. 2. Model Number (REF): 782112
FDA Device · Class II · 2026-05-06 · Philips North America - Philips Evolution Upgrade 1.5T with MR Elastography (MRE). 1. Model Number (REF): 782116 2. Model Number (REF): 782148. 3. Model Number (RE…
FDA Device · Class II · 2026-05-06 · Philips North America - Spectral CT 7500 on Rails
FDA Device · Class II · 2026-02-18 · Philips North America - IQon Spectral CT
FDA Device · Class II · 2026-02-18 · Philips North America - Spectral CT
FDA Device · Class II · 2026-02-18 · Philips North America - Brilliance iCT
FDA Device · Class II · 2026-02-18 · Philips North America - Ingenia 1.5T. Product Code (REF): (1) 781341, (2) 781396
FDA Device · Class II · 2026-02-04 · Philips North America - SmartPath to dStream for XR and 3.0T. Product Code (REF): 781270
FDA Device · Class II · 2026-02-04 · Philips North America - MR 7700
FDA Device · Class II · 2026-02-04 · Philips North America - Ingenia Ambition X. Product Code (REF): (1) 781356, (2) 782109, (3)782138
FDA Device · Class II · 2026-02-04 · Philips North America - Upgrade to MR 7700
FDA Device · Class II · 2026-02-04 · Philips North America - Ingenia Elition S. Product Code (REF): (1) 781357, (2) 782106, (3)782137
FDA Device · Class II · 2026-02-04 · Philips North America - SmartPath to dStream for 3.0T. Product Code (REF): 782145
FDA Device · Class II · 2026-02-04 · Philips North America - Ingenia Ambition S. Product Code (REF): 782108
FDA Device · Class II · 2026-02-04 · Philips North America - Evolution Upgrade 3.0T. Product Code (REF): 782143
FDA Device · Class II · 2026-02-04 · Philips North America - Ingenia Elition X. Product Code (REF): (1) 781358, (2) 782107, (3) 782136
FDA Device · Class II · 2026-02-04 · Philips North America - Ingenia 3.0T. Product Code (REF): (1) 781342, (2) 781377
FDA Device · Class II · 2026-02-04 · Philips North America - Evolution Upgrade 1.5T. Product Codes (REF): (1) 782148, (2) 782116
FDA Device · Class II · 2026-02-04 · Philips North America - Ingenia 3.0T CX. Product Code (REF): 781271
FDA Device · Class II · 2026-02-04 · Philips North America - Patient Information Center iX
FDA Device · Class II · 2026-01-28 · Philips North America - Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor
FDA Device · Class II · 2026-01-14 · Philips North America - Azurion R3.0. Model Number 722234
FDA Device · Class II · 2025-12-17 · Philips North America - IntelliVue MP2. Product Number: M8102A
FDA Device · Class II · 2025-12-10 · Philips North America - IntelliVue Patient Monitor MX550
FDA Device · Class II · 2025-12-10 · Philips North America - IntelliVue MP70
FDA Device · Class II · 2025-12-10 · Philips North America - IntelliVue MP80
FDA Device · Class II · 2025-12-10 · Philips North America - IntelliVue Patient Monitor MX400
FDA Device · Class II · 2025-12-10 · Philips North America