Philips North America recalls

65 recalls on record · latest: April 14, 2026

Official U.S. recall history for Philips North America, compiled from official government records.

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Philips North America recalls Philips SmartPath to dStream for 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781260. 2. Model Number (REF):…

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips SmartPath to dStream for XR and 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781270. 2. Model Number…

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Ingenia Ambition X with MR Elastography (MRE). 1. Model Number (REF): 781356. 2. Model Number (REF): 782109. 3.…

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Upgrade to MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782130.

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Ingenia Elition S with MR Elastography (MRE). 1. Model Number (REF): 781357. 2. Model Number (REF): 782106. 3.…

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Evolution Upgrade 1.5T with MR Elastography (MRE). 1. Model Number (REF): 782116 2. Model Number (REF): 782148.…

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Achieva 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781278.

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782120. 2. Model Number (REF): 782153.

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Ingenia 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781315. 2. Model Number (REF): 781341. 3. Model…

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Achieva 1.5T Initial system with MR Elastography (MRE). 1. Model Number (REF): 781178.

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Ingenia 3.0T CX with MR Elastography (MRE). 1. Model Number (REF): 781271. 2. Model Number (REF): 782105. 510(k…

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF): 781358. 2. Model Number (REF): 782107. 3.…

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Ingenia 1.5T CX with MR Elastography (MRE). 1. Model Number (REF): 781262.

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Achieva 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781196. 2. Model Number (REF): 781296.

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Ingenia Ambition S with MR Elastography (MRE). 1. Model Number (REF): 781359. 2. Model Number (REF): 782108. 3.…

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Evolution upgrade 3.0T with MR Elastography (MRE). 1. Model Number (REF): 782143. 2. Model Number (REF): 782162.

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Ingenia 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781342. 2. Model Number (REF): 781377. 3. Model…

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips SmartPath to Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF): 782118. 2. Model Number (REF)…

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips SmartPath to dStream for 3.0T with MR Elastography (MRE). 1. Model Number (REF): 782145.

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Patient Information Center iX; Software Version Number: 4.5.0

December 22, 2025 · Medical device recalls Moderate risk A recent software (SW) patch modifies Mobile Event Notification filter settings…

Philips North America recalls Ingenia 1.5T. Product Code (REF): (1) 781341, (2) 781396. MR systems with SW version R11.1 and R12.1.

December 3, 2025 · Medical device recalls Moderate risk The potential for stiffness value errors when viewing exported MR Elastography…

Philips North America recalls Upgrade to MR 7700. Product Code (REF): 782130. MR systems with SW version R11.1 and R12.1.

December 3, 2025 · Medical device recalls Moderate risk The potential for stiffness value errors when viewing exported MR Elastography…

Philips North America recalls Ingenia Elition S. Product Code (REF): (1) 781357, (2) 782106, (3)782137. MR systems with SW version R11.1 and R12.1.

December 3, 2025 · Medical device recalls Moderate risk The potential for stiffness value errors when viewing exported MR Elastography…

Philips North America recalls Ingenia Ambition X. Product Code (REF): (1) 781356, (2) 782109, (3)782138. MR systems with SW version R11.1 and R12.1.

December 3, 2025 · Medical device recalls Moderate risk The potential for stiffness value errors when viewing exported MR Elastography…

Philips North America recalls SmartPath to dStream for XR and 3.0T. Product Code (REF): 781270. MR systems with SW version R11.1 and R12.1.

December 3, 2025 · Medical device recalls Moderate risk The potential for stiffness value errors when viewing exported MR Elastography…

Philips North America recalls Evolution Upgrade 3.0T. Product Code (REF): 782143. MR systems with SW version R11.1 and R12.1.

December 3, 2025 · Medical device recalls Moderate risk The potential for stiffness value errors when viewing exported MR Elastography…

Philips North America recalls Ingenia Elition X. Product Code (REF): (1) 781358, (2) 782107, (3) 782136. MR systems with SW version R11.1 and R12.1.

December 3, 2025 · Medical device recalls Moderate risk The potential for stiffness value errors when viewing exported MR Elastography…

Philips North America recalls Ingenia 3.0T CX. Product Code (REF): 781271. MR systems with SW version R11.1 and R12.1.

December 3, 2025 · Medical device recalls Moderate risk The potential for stiffness value errors when viewing exported MR Elastography…

Philips North America recalls MR 7700. Product Code (REF): (1) 782120, (2) 782153. MR systems with SW version R11.1 and R12.1.

December 3, 2025 · Medical device recalls Moderate risk The potential for stiffness value errors when viewing exported MR Elastography…

Philips North America recalls Ingenia 3.0T. Product Code (REF): (1) 781342, (2) 781377. MR systems with SW version R11.1 and R12.1.

December 3, 2025 · Medical device recalls Moderate risk The potential for stiffness value errors when viewing exported MR Elastography…

Philips North America recalls Evolution Upgrade 1.5T. Product Codes (REF): (1) 782148, (2) 782116. MR systems with SW version R11.1 and R12.1.

December 3, 2025 · Medical device recalls Moderate risk The potential for stiffness value errors when viewing exported MR Elastography…

Philips North America recalls Ingenia Ambition S. Product Code (REF): 782108. MR systems with SW version R11.1 and R12.1.

December 3, 2025 · Medical device recalls Moderate risk The potential for stiffness value errors when viewing exported MR Elastography…

Philips North America recalls SmartPath to dStream for 3.0T. Product Code (REF): 782145. MR systems with SW version R11.1 and R12.1.

December 3, 2025 · Medical device recalls Moderate risk The potential for stiffness value errors when viewing exported MR Elastography…

Philips North America recalls Azurion R3.0. Model Number 722234. Commercial Name: Azurion 7 M20. INTERVENTIONAL FLUOROSCOPIC XRAY SYSTEM

October 27, 2025 · Medical device recalls Moderate risk Between July 2024 and June 2025, Philips Azurion R3.0 systems with a FlexArm st…

Philips North America recalls Cardiac Workstation 7000; Model Number: 860441;

September 12, 2025 · Medical device recalls Moderate risk Failure of Environmental Stress Testing from a pinched power module wire within…

Philips North America recalls Cardiac Workstation 5000; Model Number: 860439;

September 12, 2025 · Medical device recalls Moderate risk Failure of Environmental Stress Testing from a pinched power module wire within…

Ingenia Ambition X recalled over fire hazard

June 30, 2025 · Medical device recalls Moderate risk The potential for component failures in the Gradient Coil of the affected MR sy…

Philips North America product recalled over fire hazard

June 30, 2025 · Medical device recalls Moderate risk The potential for component failures in the Gradient Coil of the affected MR sy…

SmartPath to dStream for XR and 3 recalled over fire hazard

June 30, 2025 · Medical device recalls Moderate risk The potential for component failures in the Gradient Coil of the affected MR sy…

Ingenia 1 recalled over fire hazard

June 30, 2025 · Medical device recalls Moderate risk The potential for component failures in the Gradient Coil of the affected MR sy…

Intera 3 recalled over fire hazard

June 30, 2025 · Medical device recalls Moderate risk The potential for component failures in the Gradient Coil of the affected MR sy…

Evolution Upgrade 1 recalled over fire hazard

June 30, 2025 · Medical device recalls Moderate risk The potential for component failures in the Gradient Coil of the affected MR sy…

Evolution Upgrade 3 recalled over fire hazard

June 30, 2025 · Medical device recalls Moderate risk The potential for component failures in the Gradient Coil of the affected MR sy…

SmartPath to Ingenia Elition X recalled over fire hazard

June 30, 2025 · Medical device recalls Moderate risk The potential for component failures in the Gradient Coil of the affected MR sy…

Achieva XR recalled over fire hazard

June 30, 2025 · Medical device recalls Moderate risk The potential for component failures in the Gradient Coil of the affected MR sy…

Ingenia Elition S recalled over fire hazard

June 30, 2025 · Medical device recalls Moderate risk The potential for component failures in the Gradient Coil of the affected MR sy…

Ingenia 3 recalled over fire hazard

June 30, 2025 · Medical device recalls Moderate risk The potential for component failures in the Gradient Coil of the affected MR sy…

Upgrade to MR 7700 recalled over fire hazard

June 30, 2025 · Medical device recalls Moderate risk The potential for component failures in the Gradient Coil of the affected MR sy…

Achieva 3 recalled over fire hazard

June 30, 2025 · Medical device recalls Moderate risk The potential for component failures in the Gradient Coil of the affected MR sy…

Ingenia Ambition S recalled over fire hazard

June 30, 2025 · Medical device recalls Moderate risk The potential for component failures in the Gradient Coil of the affected MR sy…

Philips North America product recalled over fire hazard

June 30, 2025 · Medical device recalls Moderate risk The potential for component failures in the Gradient Coil of the affected MR sy…

Ingenia 3 recalled over fire hazard

June 30, 2025 · Medical device recalls Moderate risk The potential for component failures in the Gradient Coil of the affected MR sy…

Ingenia 1 recalled over fire hazard

June 30, 2025 · Medical device recalls Moderate risk The potential for component failures in the Gradient Coil of the affected MR sy…

SmartPath to dStream for 3 recalled over fire hazard

June 30, 2025 · Medical device recalls Moderate risk The potential for component failures in the Gradient Coil of the affected MR sy…

Ingenia Elition X recalled over fire hazard

June 30, 2025 · Medical device recalls Moderate risk The potential for component failures in the Gradient Coil of the affected MR sy…

Achieva XR Product Numbers recalled over fire hazard

May 29, 2025 · Medical device recalls Moderate risk identified an issue where a component failure in the specific Gradient Coil typ…

Intera 1 recalled over fire hazard

May 29, 2025 · Medical device recalls Moderate risk identified an issue where a component failure in the specific Gradient Coil typ…

Intera 1 recalled over fire hazard

May 29, 2025 · Medical device recalls Moderate risk identified an issue where a component failure in the specific Gradient Coil typ…

Intera Achieva 1 recalled over fire hazard

May 29, 2025 · Medical device recalls Moderate risk identified an issue where a component failure in the specific Gradient Coil typ…

Intera 1 recalled over fire hazard

May 29, 2025 · Medical device recalls Moderate risk identified an issue where a component failure in the specific Gradient Coil typ…

Intera 1 recalled over fire hazard

May 29, 2025 · Medical device recalls Moderate risk identified an issue where a component failure in the specific Gradient Coil typ…

SmartPath to dStream for 1 recalled over fire hazard

May 29, 2025 · Medical device recalls Moderate risk identified an issue where a component failure in the specific Gradient Coil typ…

Intera 1 recalled over fire hazard

May 29, 2025 · Medical device recalls Moderate risk identified an issue where a component failure in the specific Gradient Coil typ…

Intera 1 recalled over fire hazard

May 29, 2025 · Medical device recalls Moderate risk identified an issue where a component failure in the specific Gradient Coil typ…

Philips North America recalls IntelliVue Patient Monitor MX400 (Model Number 866060), MX430 (Model Number 866061), MX450 (Model Number 866062), MX500…

August 30, 2024 · Medical device recalls Moderate risk During a production process, Philips became aware of one IntelliVue power suppl…