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.

• The Oncology Essentials Package of the Spectral CT imaging system
  FDA Device · Class II · 2024-05-08 · Philips North America
• Philips Patient Information Center (PIC) iX Uninterruptable Power Supply (UPS): 1. APC (Schneider Electric IT Corporation) 120V Uninterrupt…
  FDA Device · Class II · 2024-05-01 · Philips North America
• Evolution Upgrade 3.0T, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Ingenia 3.0T, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• GYROSCAN ACS-NT, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Intera 1.5T, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Intera 1.5T Achieva Nova, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• SmartPath to dStream for XR and 3.0T, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Ingenia Elition X, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Achieva 3.0TX for PET, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Achieva 1.5T Conversion, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Intera Achieva 1.5T Pulsar, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• GYROSCAN T5, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Intera CV, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Intera 1.0T Power/Pulsar, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Intera 1.5T R11, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Achieva XR, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Intera 1.5T Omni/Stellar, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• MR 5300, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Achieva 1.5T Initial, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Ingenia 1.5T CX, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Intera 1.0T Omni/Stellar, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• GYROSCAN T5-NT, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Achieva 3.0T for PET, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• SmartPath to dStream for 1.5T, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• GYROSCAN T10-NT, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Ingenia 1.5T, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Intera 1.5T Achieva Nova-Dual, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Intera 1.5T Power/Pulsar, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• MR 7700, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Achieva 3.0T, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Intera 1.5T Master/Nova, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Ingenia Ambition S, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Ingenia Elition S, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Intera 3.0T Quasar Dual, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Enterprise 1.5T, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Intera 1.5T Achieva IT Nova, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Ingenia Ambition X, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Intera 0.5T Standard, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Achieva 1.5T, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Ingenia 3.0T CX, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Ingenia 1.5T S, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• Intera 1.5T Explorer/Nova Dual, Magnetic Resonance System
  FDA Device · Class II · 2024-04-24 · Philips North America
• PHILIPS Incisive Computed tomography X-ray system Incisive CT Software Upgrade from V4.5.1.41921 to V4.5.1.41989-Intended to produce cross-…
  FDA Device · Class II · 2024-04-17 · Philips North America
• CareEvent Event Management System, Model Numbers 866435 and 866436 (CareEvent Upgrade), Software Version Number C.03.X
  FDA Device · Class II · 2024-04-03 · Philips North America
• Patient Information Center iX (PIC iX), Model Numbers 866389, 866390 (PIC iX Expand), and 866424 (PIC iX Hardware) running Software Version…
  FDA Device · Class II · 2024-04-03 · Philips North America
• ProxiDiagnost upgrade- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref:706150
  FDA Device · Class II · 2024-02-21 · Philips North America
• ProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref: (1)706100 (2)706110
  FDA Device · Class II · 2024-02-21 · Philips North America
• Ingenia Elition X (Product Number 781358) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system
  FDA Device · Class II · 2024-02-14 · Philips North America
• BrightView, gamma camera system
  FDA Device · Class I · 2024-02-14 · Philips North America