Recalls from PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

• Philips Azurion (opens in a new tab)
  Moderate risk, FDA, Aug 10, 2026, Software defect
• Philips Azurion Interventional Fluoroscopic X-Ray Systems (opens in a new tab)
  Moderate risk, FDA, Aug 10, 2026, Software defect
• Philips Allura Xper FD Interventional Fluoroscopic X-Ray Systems (opens in a new tab)
  Moderate risk, FDA, Aug 10, 2026, Software defect
• Philips Allura and Azurion X-Ray Systems (opens in a new tab)
  Moderate risk, FDA, Aug 5, 2026, Device defect
• Philips MultiDiagnost Eleva and Allura Xper Systems (opens in a new tab)
  Moderate risk, FDA, Jun 16, 2026, Device defect

Data: Recall Canary (opens in a new tab)