Recalls from Siemens Medical Solutions USA, Inc

• Siemens ARTIS Icono Ceiling (opens in a new tab)
  Moderate risk, FDA, Jul 1, 2026, Device defect
• Siemens ARTIS Icono Biplane, Ceiling and Floor (opens in a new tab)
  Moderate risk, FDA, Jul 1, 2026, Device defect
• Siemens Artis Pheno and Artis Icono Interventional Fluoroscopic X-Ray Systems (opens in a new tab)
  Moderate risk, FDA, Jun 4, 2026, Device defect
• Siemens Artis Pheno Angiography Systems (opens in a new tab)
  Moderate risk, FDA, Apr 16, 2026, Device defect
• Siemens Artis Pheno and Artis Icono Biplane Systems (opens in a new tab)
  Moderate risk, FDA, Apr 7, 2026, Device defect

Data: Recall Canary (opens in a new tab)