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.

• 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
• Mammotrak Diagnostic Coil 1.5T
  FDA Device · Class II · 2024-12-04 · Philips North America
• dS Breast 16ch 3.0T
  FDA Device · Class II · 2024-12-04 · Philips North America
• dS Breast 16ch 1.5T
  FDA Device · Class II · 2024-12-04 · Philips North America
• SENSE Breast Coil 3.0T 7ch
  FDA Device · Class II · 2024-12-04 · Philips North America
• ST SENSE Breast Dx Coil
  FDA Device · Class II · 2024-12-04 · Philips North America
• IntelliVue Patient Monitor MX400/MX450/MX500/MX550 with software version P.01.01 and ordered with Option CP2 are affected as follows: 1) In…
  FDA Device · Class II · 2024-10-16 · Philips North America
• Patient Information Center iX, Product Code 866386, and Patient Information Center iX Expand, Product Code 866390, Software Revision 4.0.1
  FDA Device · Class II · 2024-10-16 · Philips North America
• IntelliVue G7m Anesthesia Gas Module, Product Number 866173
  FDA Device · Class II · 2024-10-09 · Philips North America
• DIVA 24 Inch Widescreen LCD Touch Display - Used with the Philips PIC iX system central monitoring system
  FDA Device · Class II · 2024-10-09 · Philips North America
• Ingenia 3.0T CX - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal stru…
  FDA Device · Class II · 2024-10-02 · Philips North America
• IntelliVue Patient Monitor MX400 (Model Number 866060), MX430 (Model Number 866061), MX450 (Model Number 866062), MX500 (Model Number 86606…
  FDA Device · Class II · 2024-10-02 · Philips North America
• Ingenia 3.0T - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structu…
  FDA Device · Class II · 2024-10-02 · Philips North America
• Ingenia Ambition S - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal s…
  FDA Device · Class II · 2024-10-02 · Philips North America
• Ingenia Ambition X - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal s…
  FDA Device · Class II · 2024-10-02 · Philips North America
• SmartPath to Ingenia Elition X - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of th…
  FDA Device · Class II · 2024-10-02 · Philips North America
• SmartPath to dStream for XR and 3.0T- For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra…
  FDA Device · Class II · 2024-10-02 · Philips North America
• Evolution Upgrade 3.0T - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the intern…
  FDA Device · Class II · 2024-10-02 · Philips North America
• MR 7700 -For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of…
  FDA Device · Class II · 2024-10-02 · Philips North America
• Ingenia 1.5T -For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structur…
  FDA Device · Class II · 2024-10-02 · Philips North America