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.

• 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
• Spectral CT. Computed tomography X-ray system
  FDA Device · Class II · 2025-07-02 · Philips North America
• Intera 1.5T Master/Nova Product Number: 781106
  FDA Device · Class II · 2025-06-18 · Philips North America
• Achieva XR Product Numbers: (1) 781153, (2) 781253
  FDA Device · Class II · 2025-06-18 · Philips North America
• Intera 1.5T Achieva Nova Product Number: 781172
  FDA Device · Class II · 2025-06-18 · Philips North America
• Intera 1.5T Achieva IT Nova Product Number: 781175
  FDA Device · Class II · 2025-06-18 · Philips North America
• Intera 1.5T Omni/Stellar
  FDA Device · Class II · 2025-06-18 · Philips North America
• Intera 1.5T Explorer/Nova Dual Product Number: 781108
  FDA Device · Class II · 2025-06-18 · Philips North America
• SmartPath to dStream for 1.5T¿
  FDA Device · Class II · 2025-06-18 · Philips North America
• Intera Achieva 1.5T Pulsar
  FDA Device · Class II · 2025-06-18 · Philips North America
• Intera 1.5T Achieva Nova-Dual Product Number: 781173
  FDA Device · Class II · 2025-06-18 · Philips North America
• Product Name: Evolution Upgrade 1.5T
  FDA Device · Class II · 2025-05-28 · Philips North America
• Product Name: SmartPath to Ingenia Elition X
  FDA Device · Class II · 2025-05-28 · Philips North America
• Product Name: SmartPath to dStream for 1.5T
  FDA Device · Class II · 2025-05-28 · Philips North America
• Product Name: SmartPath to dStream for 3.0T
  FDA Device · Class II · 2025-05-28 · Philips North America
• Product Name: MR 7700
  FDA Device · Class II · 2025-05-28 · Philips North America
• Product Name: Upgrade to MR 7700
  FDA Device · Class II · 2025-05-28 · Philips North America
• Product Name: Ingenia Elition X
  FDA Device · Class II · 2025-05-28 · Philips North America
• Product Name: Ingenia 3.0T
  FDA Device · Class II · 2025-05-28 · Philips North America
• Product Name: Ingenia 1.5T CX
  FDA Device · Class II · 2025-05-28 · Philips North America