Recalls from Philips North America Llc

• Philips Spectral CT 7500 (opens in a new tab)
  Moderate risk, FDA, Sep 29, 2026, Device defect
• Philips Achieva, Ingenia, Intera and MR MRI Systems (opens in a new tab)
  Moderate risk, FDA, Sep 18, 2026, Software defect
• Philips Brilliance, IQon Spectral and Ingenuity CT Scanners (opens in a new tab)
  Moderate risk, FDA, Sep 1, 2026, Device defect
• Philips Cardiac Workstation 5000 and 7000 (opens in a new tab)
  Moderate risk, FDA, Aug 14, 2026, Device defect
• Philips Telemetry Monitor 5500 1.4 GHz (opens in a new tab)
  Moderate risk, FDA, Jun 24, 2026, Labeling error

Data: Recall Canary (opens in a new tab)