Siemens Medical Solutions USA recalls

Siemens Medical Solutions USA has 796 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 8 Jul 2026. 154 are still ongoing. 19 were reported in the last 12 months. The most frequent reason is device malfunction.

Total recalls796since 2012
Last 12 months19reported
Class I162% of total
Ongoing154latest 8 Jul 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 16 2%Class II 779 98%Class III 1 0%

Why siemens medical solutions usa is recalled

By year

Ongoing siemens medical solutions usa recalls

154 active

All siemens medical solutions usa recalls, newest first

796 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIArtis icono ceiling recalled by Siemens Medical Solutions USASiemens Medical Solutions USAOtherNationwide
DeviceCLASS IIArtis icono biplane recalled by Siemens Medical Solutions USASiemens Medical Solutions USAOtherNationwide
DeviceCLASS IIArtis icono floor recalled by Siemens Medical Solutions USASiemens Medical Solutions USAOtherNationwide
DeviceCLASS IIArtis icono ceiling recalled by Siemens Medical Solutions USASiemens Medical Solutions USAOtherNationwide
DeviceCLASS IIArtis pheno recalled by Siemens Medical Solutions USASiemens Medical Solutions USAOtherPA
DeviceCLASS IIArtis Icono biplane, floor and ceiling.: Artis icono biplane recalledSiemens Medical Solutions USAOtherPA
DeviceCLASS IIArtis Pheno VE30A and VE40A recalled by Siemens Medical Solutions USASiemens Medical Solutions USAOtherPA
DeviceCLASS IIArtis pheno and Artis Icono biplane, floor and ceiling recalledSiemens Medical Solutions USAOtherNationwide
DeviceCLASS IINaeotom Alpha.Prime recalled by Siemens Medical Solutions USASiemens Medical Solutions USADevice MalfunctionNationwide
DeviceCLASS IINaeotom Alpha recalled by Siemens Medical Solutions USASiemens Medical Solutions USADevice MalfunctionNationwide
DeviceCLASS IISomatom X.ceed recalled by Siemens Medical Solutions USASiemens Medical Solutions USADevice MalfunctionNationwide
DeviceCLASS IINaeotom Alpha.Pro recalled by Siemens Medical Solutions USASiemens Medical Solutions USADevice MalfunctionNationwide
DeviceCLASS IIInterventional Fluoroscopic X-Ray System: Luminos Q.namix recalledSiemens Medical Solutions USADevice MalfunctionNationwide
DeviceCLASS IIInterventional Fluoroscopic X-Ray System: Luminos Q.namix recalledSiemens Medical Solutions USADevice MalfunctionNationwide
DeviceCLASS IILuminos Lotus Max recalled by Siemens Medical Solutions USASiemens Medical Solutions USADevice MalfunctionPA
DeviceCLASS IIMammomat Revelation recalled by Siemens Medical Solutions USASiemens Medical Solutions USAOtherNationwide
DeviceCLASS IIMammomat Fusion recalled by Siemens Medical Solutions USASiemens Medical Solutions USAOtherNationwide
DeviceCLASS IIMammomat Inspiration recalled by Siemens Medical Solutions USASiemens Medical Solutions USAOtherNationwide
DeviceCLASS IMagnetom Cima.X Upgrade recalled by Siemens Medical Solutions USASiemens Medical Solutions USAPackaging DefectsCA
DeviceCLASS IMagnetom Verio Dot recalled by Siemens Medical Solutions USASiemens Medical Solutions USAPackaging DefectsNationwide
DeviceCLASS IBiograph One (DE) recalled by Siemens Medical Solutions USASiemens Medical Solutions USAPackaging DefectsNationwide
DeviceCLASS IMagnetom Prisma recalled by Siemens Medical Solutions USASiemens Medical Solutions USAPackaging DefectsNationwide
DeviceCLASS IMagnetom Connectom.X recalled by Siemens Medical Solutions USASiemens Medical Solutions USAPackaging DefectsNationwide
DeviceCLASS IMagnetom Verio Dot Upgrade recalled by Siemens Medical Solutions USASiemens Medical Solutions USAPackaging DefectsNationwide
DeviceCLASS IMagnetom Cima.X (DE) recalled by Siemens Medical Solutions USASiemens Medical Solutions USAPackaging DefectsNationwide
DeviceCLASS IMagnetom Skyra fit recalled by Siemens Medical Solutions USASiemens Medical Solutions USAPackaging DefectsNationwide
DeviceCLASS IMagnetom Vida Fit recalled by Siemens Medical Solutions USASiemens Medical Solutions USAPackaging DefectsNationwide
DeviceCLASS IMagnetom Vida (DE) recalled by Siemens Medical Solutions USASiemens Medical Solutions USAPackaging DefectsNationwide
DeviceCLASS IMagnetom Skyra Fit BioMatrix recalled by Siemens Medical Solutions USASiemens Medical Solutions USAPackaging DefectsNationwide
DeviceCLASS IMagnetom Spectra as the following: Magnetom Spectra recalledSiemens Medical Solutions USAPackaging DefectsNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.