Philips Medical Systems Nederland B.V. recalls – page 3

• Intera 1.5T, Model Numbers: 781195 and 781295 recall
  FDA May 21, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Intera 1.0T Power/Pulsar, Model Number: 781103 recall
  FDA May 21, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Intera 1.0T Omni/Stellar, Model Number: 781102 recall
  FDA May 21, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Intera 0.5T Standard, Model Number: 781101 recall
  FDA May 21, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Enterprise 1.5T, Model Number: 781145 recall
  FDA May 21, 2025 · Philips Medical Systems Nederland B.V. · Class II
• IntelliSpace Cardiovascular software versions 6.x, 7.x, and 8.x recall
  FDA May 14, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Zenition 70. The device is to be used in health care facilities both… recall
  FDA April 30, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Spectral CT on Rails, Software Version Number 5.1.0, Model number: 728334 recall
  FDA March 19, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Philips IntelliSpace Cardiovascular software, Model 830089 recall
  FDA March 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Cardio Vascular-Allura Centron recall
  FDA February 26, 2025 · Philips Medical Systems Nederland B.V. · Class I
• Azurion 7 M20 recall
  FDA February 26, 2025 · Philips Medical Systems Nederland B.V. · Class I
• Azurion 7 M12 recall
  FDA February 26, 2025 · Philips Medical Systems Nederland B.V. · Class I
• Azurion 7 B20 recall
  FDA February 26, 2025 · Philips Medical Systems Nederland B.V. · Class I
• Azurion 7 B12 recall
  FDA February 26, 2025 · Philips Medical Systems Nederland B.V. · Class I
• Azurion 5 M20 recall
  FDA February 26, 2025 · Philips Medical Systems Nederland B.V. · Class I
• Azurion 5 M12 recall
  FDA February 26, 2025 · Philips Medical Systems Nederland B.V. · Class I
• Azurion 3 M15 recall
  FDA February 26, 2025 · Philips Medical Systems Nederland B.V. · Class I
• Azurion 3 M12 recall
  FDA February 26, 2025 · Philips Medical Systems Nederland B.V. · Class I
• Allura Xper FD10C recall
  FDA February 26, 2025 · Philips Medical Systems Nederland B.V. · Class I
• Allura CV20 recall
  FDA February 26, 2025 · Philips Medical Systems Nederland B.V. · Class I
• Allura Xper FD20/20 recall
  FDA February 26, 2025 · Philips Medical Systems Nederland B.V. · Class I
• Allura Xper FD20/15 recall
  FDA February 26, 2025 · Philips Medical Systems Nederland B.V. · Class I
• Allura Xper FD20/10 recall
  FDA February 26, 2025 · Philips Medical Systems Nederland B.V. · Class I
• Allura Xper FD20 OR Table recall
  FDA February 26, 2025 · Philips Medical Systems Nederland B.V. · Class I
• Allura Xper FD20 Biplane OR Table recall
  FDA February 26, 2025 · Philips Medical Systems Nederland B.V. · Class I
• Allura Xper FD20 Biplane recall
  FDA February 26, 2025 · Philips Medical Systems Nederland B.V. · Class I
• Allura Xper FD20 recall
  FDA February 26, 2025 · Philips Medical Systems Nederland B.V. · Class I
• Allura Xper FD10/10 recall
  FDA February 26, 2025 · Philips Medical Systems Nederland B.V. · Class I
• Allura Xper FD10 recall
  FDA February 26, 2025 · Philips Medical Systems Nederland B.V. · Class I
• Azurion 7 M20 System code: (1) 722224 (2) 722079 (3) 722234 (4) 722282… recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 7 M12 System Code: (1) 722078 (2) 722223 (3) 722233 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 7 B20 System Code: (1) 722068 (2) 722226 (3) 722236 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 7 B12 System Code: (1) 722067 (2) 722225 (3) 722235 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 5 M20 System Code: (1) 722228 (2) 722232 (3) 722281 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 5 M12 System Code: (1) 722227 (2) 722231 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 3 M15 System Code: (1) 722064 (2) 722222 (3) 722280 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Azurion 3 M12 System Code: (1) 722063 (2) 722221 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• AlluraXperFD20/15 System Code: (1) 722058 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Allura Xper FD20/20 System Code: (1) 722038 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• AlluraXperFD20/10 System Code: (1) 722029 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• AlluraXper FD20 OR Table System Code: (1) 722023 (2) 722035 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• AlluraXper FD20 Biplane OR Table System Code: (1) 722020 (2) 722025 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• AlluraXper FD20 Biplane System Code: (1) 722008 (2) 722013 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 722028 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Allura Xper FD10C System Code: (1) 722001 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• AlluraXper FD10/10 System Code: (1) 722005 (2) 722011 (3) 722027 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Allura Xper FD10 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Allura CV20 System Code: 722031 recall
  FDA February 12, 2025 · Philips Medical Systems Nederland B.V. · Class II
• Philips Allura Xper Systems (R7.6-R8.1) recall
  FDA December 18, 2024 · Philips Medical Systems Nederland B.V. · Class II
• Philips Zenition 70, Model Number: 718133 recall
  FDA November 20, 2024 · Philips Medical Systems Nederland B.V. · Class II
• Philips Zenition 50, Model Number: 718096 recall
  FDA November 20, 2024 · Philips Medical Systems Nederland B.V. · Class II