Philips North America recalls

Philips North America appears in 532 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.

• 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
• Cardiac Workstation 7000
  FDA Device · Class II · 2025-10-22 · Philips North America
• Cardiac Workstation 5000
  FDA Device · Class II · 2025-10-22 · Philips North America
• Philips CT systems labeled as the following: 1. Big Bore RT, Model Number: 728242. 2. Brilliance CT Big Bore Oncology, Model Number: 728243…
  FDA Device · Class II · 2025-10-01 · Philips North America
• Philips CT systems labeled as the following: 1. Brilliance iCT SP, Model Number: 728311
  FDA Device · Class II · 2025-10-01 · Philips North America
• Philips CT systems labeled as the following: 1. Brilliance 16 Power, Model Number: 728240. 2. Brilliance CT 16 Slice, Model Number: 728246.…
  FDA Device · Class II · 2025-10-01 · Philips North America
• Philips CT systems labeled as the following: 1. Ingenuity Core128 / Elite China, Model Number: 728324
  FDA Device · Class II · 2025-10-01 · Philips North America
• Philips CT systems labeled as the following: 1. Ingenuity CT Family Brazil, Model Number: 728325
  FDA Device · Class II · 2025-10-01 · Philips North America
• Philips CT systems labeled as the following: 1. Brilliance CT 40 Channel, Model Number: 728235. 2. Brilliance CT 64 Channel, Model Number:…
  FDA Device · Class II · 2025-10-01 · Philips North America
• Philips CT systems labeled as the following: 1. CT 6000, Model Number: 728307
  FDA Device · Class II · 2025-10-01 · Philips North America
• Philips CT systems labeled as the following: 1. Ingenuity CT 728326, Model Number: 728321. 2. Ingenuity CT 728326, Model Number: 728323. 3.…
  FDA Device · Class II · 2025-10-01 · Philips North America
• Philips CT systems labeled as the following: 1. Brilliance iCT, Model Number: 728306
  FDA Device · Class II · 2025-10-01 · Philips North America
• Philips CT systems labeled as the following: 1. IQon Spectral CT, Model Number: 728332
  FDA Device · Class II · 2025-10-01 · Philips North America
• SmartPath to dStream for XR and 3.0T Model Numbers (REF): (1) 781270, (2) 782113, (3) 782129
  FDA Device · Class II · 2025-08-06 · Philips North America
• Evolution Upgrade 1.5T Model Numbers (REF): (1) 782116, (2) 782148
  FDA Device · Class II · 2025-08-06 · Philips North America
• Ingenia 1.5T S Model Number (REF): 781347
  FDA Device · Class II · 2025-08-06 · Philips North America
• Achieva XR
  FDA Device · Class II · 2025-08-06 · Philips North America
• Ingenia 3.0T Model Numbers (REF): (1) 781342, (2) 781377, (3) 782103
  FDA Device · Class II · 2025-08-06 · Philips North America
• Ingenia 1.5T Model Numbers (REF): (1) 781315, (2) 718641, (3) 781396, (4) 782101, (5) 782115, (6) 782140
  FDA Device · Class II · 2025-08-06 · Philips North America
• SmartPath to dStream for 3.0T Model Number (REF): 782145
  FDA Device · Class II · 2025-08-06 · Philips North America
• SmartPath to Ingenia Elition X Model Numbers (REF): (1) 782118, (2) 782144
  FDA Device · Class II · 2025-08-06 · Philips North America
• Ingenia Elition S Model Numbers (REF): (1) 781357, (2) 782106, (3) 782137, (4) 782150 (China ONLY)
  FDA Device · Class II · 2025-08-06 · Philips North America
• Upgrade to MR 7700 Model Number (REF): 782130
  FDA Device · Class II · 2025-08-06 · Philips North America
• Intera 3.0T Quasar Dual Model Number (REF): 781150
  FDA Device · Class II · 2025-08-06 · Philips North America
• Ingenia Ambition S Model Numbers (REF): (1) 781359, (2) 782108, (3) 782133 (China ONLY), (4) 782139
  FDA Device · Class II · 2025-08-06 · Philips North America
• Ingenia 3.0T CX Model Numbers (REF): (1) 781271, (2) 782105
  FDA Device · Class II · 2025-08-06 · Philips North America
• MR 5300 Model Numbers (REF): (1) 782110, (2) 782135 (China ONLY), (3) 782152
  FDA Device · Class II · 2025-08-06 · Philips North America
• MR 7700 Model Numbers (REF): (1) 782120, (2) 782153
  FDA Device · Class II · 2025-08-06 · Philips North America
• Achieva 3.0T
  FDA Device · Class II · 2025-08-06 · Philips North America
• Ingenia Elition X Model Numbers (REF): (1) 781358, (2) 782107, (3) 782119, (4) 782136, (5) 782151 (China ONLY)
  FDA Device · Class II · 2025-08-06 · Philips North America
• Evolution Upgrade 3.0T Model Numbers (REF): (1) 782117, (2) 782143
  FDA Device · Class II · 2025-08-06 · Philips North America
• Ingenia Ambition X Model Numbers (REF): (1) 781356, (2) 782109, (3) 782138
  FDA Device · Class II · 2025-08-06 · Philips North America