Philips North America Llc recalls

All Philips North America Llc recalls we track from FDA, CPSC and NHTSA data. Categories: medical devices (177).

177 recalls published between October 9, 2024 and September 30, 2026. Most common issues: fire (28), software (19), burn (9), injury risk (9).

• SmartPath to dStream for 1.5T, SmartPath to dStream for 3.0T… recall
  FDA September 30, 2026 · Philips North America Llc · Class II
• MR 7700 and Upgrade to MR 7700 recall
  FDA September 30, 2026 · Philips North America Llc · Class II
• MR 5300 Model Number ( recall
  FDA September 30, 2026 · Philips North America Llc · Class II
• Name (Model Number): 1. Intera 1.5T (781195), 2. Intera 1.5T (781295), 3… recall
  FDA September 30, 2026 · Philips North America Llc · Class II
• Ingenia Elition S and Ingenia Elition X recall
  FDA September 30, 2026 · Philips North America Llc · Class II
• Ingenia 3.0T and Ingenia 3.0T CX recall
  FDA September 30, 2026 · Philips North America Llc · Class II
• Ingenia Ambition S and Ingenia Ambition X recall
  FDA September 30, 2026 · Philips North America Llc · Class II
• Ingenia 1.5T, Ingenia 1.5T CX and Ingenia 1.5T S recall
  FDA September 30, 2026 · Philips North America Llc · Class II
• Evolution upgrade 1.5T and Evolution upgrade 3.0T recall
  FDA September 30, 2026 · Philips North America Llc · Class II
• Achieva XR recall
  FDA September 30, 2026 · Philips North America Llc · Class II
• Achieva 3.0T recall
  FDA September 30, 2026 · Philips North America Llc · Class II
• Achieva 1.5T, Achieva 1.5T Conversion and Achieva 1.5T Initial system recall
  FDA September 30, 2026 · Philips North America Llc · Class II
• Philips PIC iX Essentials recall
  FDA September 23, 2026 · Philips North America Llc · Class II
• Philips Patient Information Center iX recall
  FDA September 23, 2026 · Philips North America Llc · Class II
• Philips Brilliance CT 64: Brilliance CT 64 Channel Product Code: 728231… recall
  FDA September 9, 2026 · Philips North America Llc · Class II
• Philips Ingenuity CT Product Codes: Ingenuity CT Upgrades 728327… recall
  FDA September 9, 2026 · Philips North America Llc · Class II
• Philips IQon Spectral CT Product Codes: IQon Spectral CT 728332… recall
  FDA September 9, 2026 · Philips North America Llc · Class II
• Philips Brilliance recall
  FDA September 9, 2026 · Philips North America Llc · Class II
• Cardiac Workstation 7000. Product Number: 860441 recall
  FDA August 26, 2026 · Philips North America Llc · Class II
• Cardiac Workstation 5000. Product Number: 860439 recall
  FDA August 26, 2026 · Philips North America Llc · Class II
• Philips Telemetry Monitor 5500 1.4 GHz recall
  FDA July 1, 2026 · Philips North America Llc · Class II
• Philips Avalon Fetal Monitor, FM 30 Part numberM2703A recall
  FDA July 1, 2026 · Philips North America Llc · Class II
• Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703A recall
  FDA July 1, 2026 · Philips North America Llc · Class II
• DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035 recall
  FDA June 17, 2026 · Philips North America Llc · Class II
• Philips Upgrade to MR 7700 with MR Elastography (MRE) recall
  FDA May 6, 2026 · Philips North America Llc · Class II
• Philips SmartPath to Ingenia Elition X with MR Elastography (MRE) recall
  FDA May 6, 2026 · Philips North America Llc · Class II
• Philips SmartPath to dStream for XR and 3.0T with MR Elastography (MRE) recall
  FDA May 6, 2026 · Philips North America Llc · Class II
• Philips SmartPath to dStream for 3.0T with MR Elastography (MRE) recall
  FDA May 6, 2026 · Philips North America Llc · Class II
• Philips SmartPath to dStream for 1.5T with MR Elastography (MRE) recall
  FDA May 6, 2026 · Philips North America Llc · Class II
• Philips MR 7700 with MR Elastography (MRE) recall
  FDA May 6, 2026 · Philips North America Llc · Class II
• Philips Ingenia Elition X with MR Elastography (MRE) recall
  FDA May 6, 2026 · Philips North America Llc · Class II
• Philips Ingenia Elition S with MR Elastography (MRE) recall
  FDA May 6, 2026 · Philips North America Llc · Class II
• Philips Ingenia Ambition X with MR Elastography (MRE) recall
  FDA May 6, 2026 · Philips North America Llc · Class II
• Philips Ingenia Ambition S with MR Elastography (MRE) recall
  FDA May 6, 2026 · Philips North America Llc · Class II
• Philips Ingenia 3.0T CX with MR Elastography (MRE) recall
  FDA May 6, 2026 · Philips North America Llc · Class II
• Philips Ingenia 3.0T with MR Elastography (MRE) recall
  FDA May 6, 2026 · Philips North America Llc · Class II
• Philips Ingenia 1.5T CX with MR Elastography (MRE) recall
  FDA May 6, 2026 · Philips North America Llc · Class II
• Philips Ingenia 1.5T with MR Elastography (MRE) recall
  FDA May 6, 2026 · Philips North America Llc · Class II
• Philips Evolution upgrade 3.0T with MR Elastography (MRE) recall
  FDA May 6, 2026 · Philips North America Llc · Class II
• Philips Evolution Upgrade 1.5T with MR Elastography (MRE) recall
  FDA May 6, 2026 · Philips North America Llc · Class II
• Philips Achieva 3.0T with MR Elastography (MRE) recall
  FDA May 6, 2026 · Philips North America Llc · Class II
• Philips Achieva 1.5T Initial system with MR Elastography (MRE) recall
  FDA May 6, 2026 · Philips North America Llc · Class II
• Philips Achieva 1.5T with MR Elastography (MRE) recall
  FDA May 6, 2026 · Philips North America Llc · Class II
• Spectral CT 7500 on Rails recall
  FDA February 18, 2026 · Philips North America Llc · Class II
• Spectral CT recall
  FDA February 18, 2026 · Philips North America Llc · Class II
• IQon Spectral CT recall
  FDA February 18, 2026 · Philips North America Llc · Class II
• Brilliance iCT recall
  FDA February 18, 2026 · Philips North America Llc · Class II
• SmartPath to dStream for XR and 3.0T. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• SmartPath to dStream for 3.0T. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Upgrade to MR 7700. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• MR 7700. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Ingenia Elition X. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Ingenia Elition S. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Ingenia Ambition X. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Ingenia Ambition S. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Ingenia 3.0T CX. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Ingenia 3.0T. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Ingenia 1.5T. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Evolution Upgrade 3.0T. Product Code ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II
• Evolution Upgrade 1.5T. Product Codes ( recall
  FDA February 4, 2026 · Philips North America Llc · Class II