Siemens Medical Solutions USA, Inc recalls

All Siemens Medical Solutions USA, Inc recalls we track from FDA, CPSC and NHTSA data. Categories: medical devices (42).

42 recalls published between February 5, 2025 and July 8, 2026. Most common issues: software (9), fire (2). 16 were FDA Class I, the most serious level.

• ARTIS icono ceiling recall
  FDA July 8, 2026 · Siemens Medical Solutions USA, Inc · Class II
• ARTIS icono floor recall
  FDA July 8, 2026 · Siemens Medical Solutions USA, Inc · Class II
• ARTIS icono ceiling recall
  FDA July 8, 2026 · Siemens Medical Solutions USA, Inc · Class II
• ARTIS icono biplane recall
  FDA July 8, 2026 · Siemens Medical Solutions USA, Inc · Class II
• ARTIS Icono biplane, floor and ceiling.: ARTIS icono biplane Model… recall
  FDA June 10, 2026 · Siemens Medical Solutions USA, Inc · Class II
• ARTIS pheno, Model 10849000. interventional fluoroscopic x-ray system recall
  FDA June 10, 2026 · Siemens Medical Solutions USA, Inc · Class II
• ARTIS Pheno VE30A and VE40A, Model 10849000 recall
  FDA April 22, 2026 · Siemens Medical Solutions USA, Inc · Class II
• ARTIS pheno and ARTIS Icono biplane, floor and ceiling recall
  FDA April 15, 2026 · Siemens Medical Solutions USA, Inc · Class II
• NAEOTOM Alpha.Pro Software applications: syngo.CT Brain Quantification… recall
  FDA February 11, 2026 · Siemens Medical Solutions USA, Inc · Class II
• NAEOTOM Alpha.Prime Software applications: syngo.CT Brain Quantification… recall
  FDA February 11, 2026 · Siemens Medical Solutions USA, Inc · Class II
• NAEOTOM Alpha Software applications: syngo.CT Brain Quantification… recall
  FDA February 11, 2026 · Siemens Medical Solutions USA, Inc · Class II
• SOMATOM X.ceed Software applications: syngo.CT Brain Quantification… recall
  FDA February 11, 2026 · Siemens Medical Solutions USA, Inc · Class II
• Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix T recall
  FDA February 4, 2026 · Siemens Medical Solutions USA, Inc · Class II
• Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R recall
  FDA February 4, 2026 · Siemens Medical Solutions USA, Inc · Class II
• LUMINOS Lotus Max, Model 11574100 and Luminos dRF Max, Model 10762471 recall
  FDA January 14, 2026 · Siemens Medical Solutions USA, Inc · Class II
• MAMMOMAT Fusion recall
  FDA December 10, 2025 · Siemens Medical Solutions USA, Inc · Class II
• MAMMOMAT Inspiration recall
  FDA December 10, 2025 · Siemens Medical Solutions USA, Inc · Class II
• MAMMOMAT Revelation recall
  FDA December 10, 2025 · Siemens Medical Solutions USA, Inc · Class II
• MAGNETOM Cima.X Upgrade recall
  FDA November 19, 2025 · Siemens Medical Solutions USA, Inc · Class I
• MAGNETOM Vida Fit recall
  FDA October 8, 2025 · Siemens Medical Solutions USA, Inc · Class I
• MAGNETOM Vida (DE) recall
  FDA October 8, 2025 · Siemens Medical Solutions USA, Inc · Class I
• MAGNETOM Verio Dot Upgrade recall
  FDA October 8, 2025 · Siemens Medical Solutions USA, Inc · Class I
• MAGNETOM Verio Dot recall
  FDA October 8, 2025 · Siemens Medical Solutions USA, Inc · Class I
• MAGNETOM Verio recall
  FDA October 8, 2025 · Siemens Medical Solutions USA, Inc · Class I
• MAGNETOM Spectra as the following: 1. MAGNETOM Spectra recall
  FDA October 8, 2025 · Siemens Medical Solutions USA, Inc · Class I
• MAGNETOM Skyra Fit BioMatrix recall
  FDA October 8, 2025 · Siemens Medical Solutions USA, Inc · Class I
• MAGNETOM Skyra fit recall
  FDA October 8, 2025 · Siemens Medical Solutions USA, Inc · Class I
• MAGNETOM Skyra (DE) recall
  FDA October 8, 2025 · Siemens Medical Solutions USA, Inc · Class I
• MAGNETOM Prisma recall
  FDA October 8, 2025 · Siemens Medical Solutions USA, Inc · Class I
• MAGNETOM Lumina (DE) recall
  FDA October 8, 2025 · Siemens Medical Solutions USA, Inc · Class I
• MAGNETOM Connectom.X. Model Number: 11371480 recall
  FDA October 8, 2025 · Siemens Medical Solutions USA, Inc · Class I
• MAGNETOM Cima.X (DE) recall
  FDA October 8, 2025 · Siemens Medical Solutions USA, Inc · Class I
• BIOGRAPH One (DE) recall
  FDA October 8, 2025 · Siemens Medical Solutions USA, Inc · Class I
• Biograph mMR. Model Number: 10433372 recall
  FDA October 8, 2025 · Siemens Medical Solutions USA, Inc · Class I
• Artis Pheno recall
  FDA September 17, 2025 · Siemens Medical Solutions USA, Inc · Class II
• interventional fluoroscopic x-ray system recall
  FDA July 9, 2025 · Siemens Medical Solutions USA, Inc · Class II
• interventional fluoroscopic x-ray system recall
  FDA July 9, 2025 · Siemens Medical Solutions USA, Inc · Class II
• interventional fluoroscopic x-ray system recall
  FDA July 9, 2025 · Siemens Medical Solutions USA, Inc · Class II
• ARTIS is a family of dedicated angiography systems developed for single… recall
  FDA July 9, 2025 · Siemens Medical Solutions USA, Inc · Class II
• UROSKOP Omnia Max recall
  FDA June 25, 2025 · Siemens Medical Solutions USA, Inc · Class II
• UROSKOP Omnia recall
  FDA June 25, 2025 · Siemens Medical Solutions USA, Inc · Class II
• ARTIS One Angiographic X-Ray System recall
  FDA February 5, 2025 · Siemens Medical Solutions USA, Inc · Class II