Philips North America recalls

Philips North America appears in 563 official U.S. recall notices indexed by RecallRadar.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• 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
• IntelliVue Patient Monitor MX450
  FDA Device · Class II · 2025-12-10 · Philips North America
• Incisive CT
  FDA Device · Class II · 2025-12-10 · Philips North America
• IntelliVue MP30
  FDA Device · Class II · 2025-12-10 · Philips North America
• IntelliVue MP50
  FDA Device · Class II · 2025-12-10 · Philips North America
• IntelliVue Patient Monitor MX500
  FDA Device · Class II · 2025-12-10 · Philips North America
• IntelliVue Multi Measurement Server X2. Product Number: M3002A
  FDA Device · Class II · 2025-12-10 · Philips North America
• IntelliVue Patient Monitor MX800
  FDA Device · Class II · 2025-12-10 · Philips North America
• IntelliVue MP5. Product Number: M8105A
  FDA Device · Class II · 2025-12-10 · Philips North America
• IntelliVue Patient Monitor MX850
  FDA Device · Class II · 2025-12-10 · Philips North America
• IntelliVue Patient Monitor MX700
  FDA Device · Class II · 2025-12-10 · Philips North America
• IntelliVue MP20
  FDA Device · Class II · 2025-12-10 · Philips North America
• IntelliVue MP60
  FDA Device · Class II · 2025-12-10 · Philips North America
• IntelliVue Patient Monitor MX100
  FDA Device · Class II · 2025-12-10 · Philips North America
• IntelliVue Patient Monitor MX750
  FDA Device · Class II · 2025-12-10 · Philips North America
• IntelliVue Patient Monitor MX600
  FDA Device · Class II · 2025-12-10 · Philips North America
• IntelliVue MP40
  FDA Device · Class II · 2025-12-10 · Philips North America
• IntelliVue Multi-Measurement Module X3. Product Number: 867030
  FDA Device · Class II · 2025-12-10 · Philips North America
• IntelliVue MP90
  FDA Device · Class II · 2025-12-10 · Philips North America
• CT 5300
  FDA Device · Class II · 2025-12-10 · Philips North America