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.

• 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
• Product Name: Ingenia Ambition X
  FDA Device · Class II · 2025-05-28 · Philips North America
• Product Name: Ingenia 3.0T CX
  FDA Device · Class II · 2025-05-28 · Philips North America
• Product Name: Ingenia 1.5T S
  FDA Device · Class II · 2025-05-28 · Philips North America
• Product Name: Ingenia Elition S
  FDA Device · Class II · 2025-05-28 · Philips North America
• Product Name: Evolution Upgrade 3.0T
  FDA Device · Class II · 2025-05-28 · Philips North America
• Product Name: Ingenia 1.5T
  FDA Device · Class II · 2025-05-28 · Philips North America
• Product Name: SmartPath to dStream for XR and 3.0T
  FDA Device · Class II · 2025-05-28 · Philips North America
• Product Name: Ingenia Ambition S
  FDA Device · Class II · 2025-05-28 · Philips North America
• Product Name: MR 5300
  FDA Device · Class II · 2025-05-28 · Philips North America
• Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as Adt/Pedi Intub CO2 Line STerm , Adt/Pedi Intub CO2 Line STerm Lng…
  FDA Device · Class II · 2025-05-14 · Philips North America
• Zenition 50
  FDA Device · Class II · 2025-04-30 · Philips North America
• Philips Brilliance CT Big Bore, Software Version 4.8.0.10430
  FDA Device · Class II · 2025-04-30 · Philips North America
• Veradius Unity
  FDA Device · Class II · 2025-04-30 · Philips North America
• Zenition 70
  FDA Device · Class II · 2025-04-30 · Philips North America
• Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System
  FDA Device · Class II · 2025-04-23 · Philips North America
• Philips DXR System, DuraDiagnost 4.1. Stationary X-Ray System
  FDA Device · Class II · 2025-04-23 · Philips North America
• IntelliVue Patient Monitor MX550
  FDA Device · Class II · 2025-02-12 · Philips North America
• IntelliVue Patient Monitor MX400
  FDA Device · Class II · 2025-02-12 · Philips North America
• IntelliVue Patient Monitor MX500
  FDA Device · Class II · 2025-02-12 · Philips North America
• IntelliBridge EC10 Module
  FDA Device · Class II · 2025-02-12 · Philips North America
• IntelliVue Patient Monitor MX450
  FDA Device · Class II · 2025-02-12 · Philips North America
• Philips Smart-Hopping 2.0 AP 1.4 GHz. Model Number: 867216
  FDA Device · Class II · 2024-12-25 · Philips North America
• Spectral CT and Spectral CT Plus
  FDA Device · Class II · 2024-12-11 · Philips North America
• Achieva TX Interventional Coil 3.0T
  FDA Device · Class II · 2024-12-04 · Philips North America
• ST SENSE Breast Coil
  FDA Device · Class II · 2024-12-04 · Philips North America
• dS Breast 7ch 1.5T
  FDA Device · Class II · 2024-12-04 · Philips North America
• Mammotrak Interventional Coil 3.0T
  FDA Device · Class II · 2024-12-04 · Philips North America
• dS Breast 7ch 3.0T
  FDA Device · Class II · 2024-12-04 · Philips North America
• Mammotrak Diagnostic Coil 3.0T
  FDA Device · Class II · 2024-12-04 · Philips North America
• Mammotrak Interventional Coil 1.5T
  FDA Device · Class II · 2024-12-04 · Philips North America
• SENSE Breast Coil
  FDA Device · Class II · 2024-12-04 · Philips North America