Philips Medical Systems Nederland B.V. recalls

All Philips Medical Systems Nederland B.V. recalls we track from FDA, CPSC and NHTSA data. Categories: medical devices (171).

171 recalls published between November 20, 2024 and August 19, 2026. Most common issues: injury risk (33), fall (20), entrapment (19), laceration (14). 20 were FDA Class I, the most serious level.

• Philips Azurion, Model Numbers: 722229, 722230, 722231, 722232, 722233… recall
  FDA August 19, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Azurion Rystem, Model Numbers: 722063, 722064, 722067, 722068… recall
  FDA August 19, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035… recall
  FDA August 19, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Allura, Cardio Vascular-Allura Centron recall
  FDA August 12, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Azurion under the following System Descriptions and corresponding… recall
  FDA August 12, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Allura under the following System Descriptions and corresponding… recall
  FDA August 12, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Allura Xper with the following Model Numbers: Model # 722001 for… recall
  FDA June 24, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips MultiDiagnost Eleva with the following Model Numbers: Model #… recall
  FDA June 24, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Azurion 7M20, Model Numbers: 722079… recall
  FDA June 10, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Azurion 7M12, Model Numbers: 722078… recall
  FDA June 10, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Azurion 7B20/15, Model Numbers: 722068… recall
  FDA June 10, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Azurion 7B12/12, Model Numbers: 722067… recall
  FDA June 10, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Azurion 5M20, Model Numbers: 722228 with Software release R2.2.0… recall
  FDA June 10, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Azurion 5M12, Model Numbers: 722227 with Software release R2.2.0… recall
  FDA June 10, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Azurion 3M15, Model Numbers: 722064… recall
  FDA June 10, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Azurion 3M12, Model Numbers: 722063… recall
  FDA June 10, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Allura system recall
  FDA June 3, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion system recall
  FDA June 3, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Integris-Allura system recall
  FDA May 27, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Allura system recall
  FDA May 27, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion system recall
  FDA May 27, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Azurion systems not configured with an optional auxiliary pan… recall
  FDA May 27, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Azurion recall
  FDA May 20, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips AneurysmFlow recall
  FDA April 22, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Vue Motion V12. Product Number: 1017979 recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 5 M20 recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 5 M12 recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 7 M20 recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 7 M12 recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 7 B20 recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 7 B12 recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 3 M15 recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 3 M12 recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Allura Xper FD20/15 OR Table recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Allura Xper FD20/15 recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Allura Xper FD20/20 OR Table recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Allura Xper FD20/20 recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Allura Xper FD20/10 recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• ALLURA Xper FD10 OR Table recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• ALLURA Xper FD20 Biplane OR Table recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• ALLURA Xper FD20 OR Table recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• ALLURA Xper FD20 Biplane recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• ALLURA Xper FD20 recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• ALLURA Xper FD10/10 recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• ALLURA Xper FD10 recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• ALLURA Xper FD10F recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Allura Xper FD10C recall
  FDA April 8, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 5 M20 System Model Numbers: (1)722228, (2)722232… recall
  FDA February 18, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 5 M12 System Model Numbers: (1)722227, (2)722231 recall
  FDA February 18, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 7 M20 System Model Numbers: (1)722079, (2)722224, (3)722234… recall
  FDA February 18, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 7 M12 System Model Numbers: (1)722078, (2)722223, (3)722233 recall
  FDA February 18, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 7 B20 System Model Numbers: (1)722068, (2)722226, (3)722236 recall
  FDA February 18, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 7 B12 System Model Numbers:(1) 722067, (2) 722225, (3) 722235 recall
  FDA February 18, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 3 M15 System Model Numbers: (1) 722064, (2) 722222, (3) 722230… recall
  FDA February 18, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 3 M12 System Model Numbers: (1) 722063, (2) 722221, (3) 722229 recall
  FDA February 18, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Azurion system recall
  FDA January 28, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Azurion Systems with software versions R2.1.10 and R2.2.10… recall
  FDA January 21, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Philips Azurion Systems R3.0. Includes the following label descriptions… recall
  FDA January 21, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Allura Xper FD20/20 recall
  FDA January 21, 2026 · Philips Medical Systems Nederland B.V. · Class II
• Allura Xper FD20/10 recall
  FDA January 21, 2026 · Philips Medical Systems Nederland B.V. · Class II