Siemens Medical Solutions USA, Inc recalls
15 recalls.
- ARTIS icono ceiling. Model Number: 11328100. recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported July 8, 2026 · Potential issue with the Display ceiling suspension (DCS Fix XL) that holds the monitor in place. Over time some screws that keep the monitor attached to the... - ARTIS icono floor. Model Number: 11327700. recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported July 8, 2026 · Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits. - ARTIS icono ceiling. Model Number: 11328100. recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported July 8, 2026 · Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits. - ARTIS icono biplane. Model Number: 11327600. recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported July 8, 2026 · Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits. - ARTIS Icono biplane recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported June 10, 2026 · During patient examinations, the system may sporadically display a 0 x-ray dose administered to the patient. This behavior has only been observed during... - ARTIS pheno recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported June 10, 2026 · During patient examinations, the system may sporadically display a 0 x-ray dose administered to the patient. This behavior has only been observed during... - ARTIS Pheno VE30A and VE40A recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported April 22, 2026 · During 3D acquisitions, lighter and darker patient images may be captured, which may result in less accurate 3D reconstruction. The variation of brightness is... - ARTIS pheno and ARTIS Icono biplane recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported April 15, 2026 · During patient examinations, the system may sporadically display a major increase of the x-ray dose applied to the patient. Despite the reported dose showing... - NAEOTOM Alpha.Pro Software applications: syngo.CT Brain Quantification syngo.CT... recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported February 11, 2026 · To remove the software applications from certain CT systems as the applications have not received FDA 510(k) clearance. - NAEOTOM Alpha.Prime Software applications: syngo.CT Brain Quantification syngo.CT... recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported February 11, 2026 · To remove the software applications from certain CT systems as the applications have not received FDA 510(k) clearance. - NAEOTOM Alpha Software applications: syngo.CT Brain Quantification syngo.CT Vessel... recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported February 11, 2026 · To remove the software applications from certain CT systems as the applications have not received FDA 510(k) clearance. - SOMATOM X.ceed Software applications: syngo.CT Brain Quantification syngo.CT... recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported February 11, 2026 · To remove the software applications from certain CT systems as the applications have not received FDA 510(k) clearance. - Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix T recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported February 4, 2026 · Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image of a... - Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported February 4, 2026 · Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image of a... - LUMINOS Lotus Max recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported January 14, 2026 · A potential issue associated with LUMINOS Lotus Max and Luminos dRF Max systems with software version VF11 with bucky wall stand for mobile detectors and...