Siemens Medical Solutions USA, Inc recalls

47 recalls on record · latest: March 12, 2026

Official U.S. recall history for Siemens Medical Solutions USA, Inc, compiled from official government records.

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Siemens Medical Solutions USA, Inc recalls ARTIS Pheno VE30A and VE40A, Model 10849000

March 12, 2026 · Medical device recalls Moderate risk During 3D acquisitions, lighter and darker patient images may be captured, whic…

Siemens Medical Solutions USA, Inc recalls ARTIS pheno and ARTIS Icono biplane, floor and ceiling. Model Numbers 10849000, 11327600, 11328100, 11327700.

March 10, 2026 · Medical device recalls Moderate risk During patient examinations, the system may sporadically display a major increa…

Siemens Medical Solutions USA, Inc recalls Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix T; Siemens Material Number (SMN): 11574003; With Software Ver…

December 29, 2025 · Medical device recalls Moderate risk Ortho images acquired with preset automatic horizontal flip are not flipped and…

Siemens Medical Solutions USA, Inc recalls Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R; Siemens Material Number (SMN): 11574002; With Software Ver…

December 29, 2025 · Medical device recalls Moderate risk Ortho images acquired with preset automatic horizontal flip are not flipped and…

Siemens Medical Solutions USA, Inc recalls NAEOTOM Alpha.Prime Software applications: syngo.CT Brain Quantification syngo.CT Vessel Hyperdensities syngo.CT ASPECTS

December 19, 2025 · Medical device recalls Moderate risk To remove the software applications from certain CT systems as the applications…

Siemens Medical Solutions USA, Inc recalls NAEOTOM Alpha Software applications: syngo.CT Brain Quantification syngo.CT Vessel Hyperdensities syngo.CT ASPECTS

December 19, 2025 · Medical device recalls Moderate risk To remove the software applications from certain CT systems as the applications…

Siemens Medical Solutions USA, Inc recalls SOMATOM X.ceed Software applications: syngo.CT Brain Quantification syngo.CT Vessel Hyperdensities syngo.CT ASPECTS

December 19, 2025 · Medical device recalls Moderate risk To remove the software applications from certain CT systems as the applications…

Siemens Medical Solutions USA, Inc recalls NAEOTOM Alpha.Pro Software applications: syngo.CT Brain Quantification syngo.CT Vessel Hyperdensities syngo.CT ASPECTS

December 19, 2025 · Medical device recalls Moderate risk To remove the software applications from certain CT systems as the applications…

Siemens Medical Solutions USA, Inc recalls LUMINOS Lotus Max, Model 11574100 and Luminos dRF Max, Model 10762471

December 5, 2025 · Medical device recalls Moderate risk A potential issue associated with LUMINOS Lotus Max and Luminos dRF Max systems…

Siemens Medical Solutions USA, Inc recalls MAMMOMAT Revelation;

October 24, 2025 · Medical device recalls Moderate risk There were instances where the operator table was sold together with a bus-inst…

Siemens Medical Solutions USA, Inc recalls MAMMOMAT Fusion;

October 24, 2025 · Medical device recalls Moderate risk There were instances where the operator table was sold together with a bus-inst…

Siemens Medical Solutions USA, Inc recalls MAMMOMAT Inspiration;

October 24, 2025 · Medical device recalls Moderate risk There were instances where the operator table was sold together with a bus-inst…

Siemens Medical Solutions USA, Inc recalls MAGNETOM Cima.X Upgrade. Model Number: 11689304.

October 1, 2025 · Medical device recalls High risk There is a potential for an ice blockage to form or currently exist within the…

Siemens Medical Solutions USA, Inc recalls MAGNETOM Verio Dot. Model Number: 10684333.

August 28, 2025 · Medical device recalls High risk There is a potential for an ice blockage to form or currently exist within the…

Siemens Medical Solutions USA, Inc recalls BIOGRAPH One (DE). Model Number: 11689172.

August 28, 2025 · Medical device recalls High risk There is a potential for an ice blockage to form or currently exist within the…

Siemens Medical Solutions USA, Inc recalls MAGNETOM Prisma. Model Number: 10849582.

August 28, 2025 · Medical device recalls High risk There is a potential for an ice blockage to form or currently exist within the…

Siemens Medical Solutions USA, Inc recalls MAGNETOM Connectom.X. Model Number: 11371480.

August 28, 2025 · Medical device recalls High risk There is a potential for an ice blockage to form or currently exist within the…

Siemens Medical Solutions USA, Inc recalls MAGNETOM Verio Dot Upgrade. Model Number: 10684334.

August 28, 2025 · Medical device recalls High risk There is a potential for an ice blockage to form or currently exist within the…

Siemens Medical Solutions USA, Inc recalls MAGNETOM Cima.X (DE). Model Number: 11647158.

August 28, 2025 · Medical device recalls High risk There is a potential for an ice blockage to form or currently exist within the…

Siemens Medical Solutions USA, Inc recalls MAGNETOM Skyra fit. Model Number: 10849580.

August 28, 2025 · Medical device recalls High risk There is a potential for an ice blockage to form or currently exist within the…

Siemens Medical Solutions USA, Inc recalls MAGNETOM Vida Fit. Model Number: 11410481.

August 28, 2025 · Medical device recalls High risk There is a potential for an ice blockage to form or currently exist within the…

Siemens Medical Solutions USA, Inc recalls MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396, K173617, K181433, K183254, K192924, K203443, K213693, K213…

August 28, 2025 · Medical device recalls High risk There is a potential for an ice blockage to form or currently exist within the…

Siemens Medical Solutions USA, Inc recalls MAGNETOM Skyra Fit BioMatrix. Model Number: 11516217.

August 28, 2025 · Medical device recalls High risk There is a potential for an ice blockage to form or currently exist within the…

Siemens Medical Solutions USA, Inc recalls MAGNETOM Spectra as the following: 1. MAGNETOM Spectra. Model Number: 10837643. 2. MAGNETOM Spectra (CN). Model Number:…

August 28, 2025 · Medical device recalls High risk There is a potential for an ice blockage to form or currently exist within the…

Siemens Medical Solutions USA, Inc recalls MAGNETOM Lumina (DE). Model Number: 11344916.

August 28, 2025 · Medical device recalls High risk There is a potential for an ice blockage to form or currently exist within the…

Siemens Medical Solutions USA, Inc recalls MAGNETOM Verio. Model Number: 10276755.

August 28, 2025 · Medical device recalls High risk There is a potential for an ice blockage to form or currently exist within the…

Siemens Medical Solutions USA, Inc recalls Biograph mMR. Model Number: 10433372.

August 28, 2025 · Medical device recalls High risk There is a potential for an ice blockage to form or currently exist within the…

Siemens Medical Solutions USA, Inc recalls MAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347, K111242, K123510, K133435, K140253, K141977, K142…

August 28, 2025 · Medical device recalls High risk There is a potential for an ice blockage to form or currently exist within the…

Siemens Medical Solutions USA, Inc recalls Artis Pheno. Image-Intensified Flouroscopic X-Ray System.

August 12, 2025 · Medical device recalls Moderate risk Limited system movements after startup .

UROSKOP Omnia recalled over fire hazard

June 4, 2025 · Medical device recalls Moderate risk A resistor in the frequency inverter may strongly overheat potentially igniting…

UROSKOP Omnia Max recalled over fire hazard

June 4, 2025 · Medical device recalls Moderate risk A resistor in the frequency inverter may strongly overheat potentially igniting…

Siemens Medical Solutions USA, Inc recalls ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and intervention…

May 15, 2025 · Medical device recalls Moderate risk In very rare situations, communication between the sensor measuring dose applie…

Siemens Medical Solutions USA, Inc recalls interventional fluoroscopic x-ray system

May 15, 2025 · Medical device recalls Moderate risk In very rare situations, communication between the sensor measuring dose applie…

Siemens Medical Solutions USA, Inc recalls interventional fluoroscopic x-ray system

May 15, 2025 · Medical device recalls Moderate risk In very rare situations, communication between the sensor measuring dose applie…

Siemens Medical Solutions USA, Inc recalls interventional fluoroscopic x-ray system

May 15, 2025 · Medical device recalls Moderate risk In very rare situations, communication between the sensor measuring dose applie…

SIEMENS MEDICAL SOLUTIONS USA, INC recalls ARTIS One Angiographic X-Ray System

January 2, 2025 · Medical device recalls Moderate risk A potential issue with ARTIS One systems was identified. In very rare situation…

Siemens Medical Solutions USA, Inc. recalls ACUSON Redwood 1.0 and 2.0 Diagnostic Ultrasound Systems, REF: 11503314, with software

August 15, 2024 · Medical device recalls Moderate risk If ultrasound systems with software, are changed from factory default to : 1) M…

Siemens Medical Solutions USA, Inc. recalls ACUSON Maple 1.0 Diagnostic Ultrasound System, REF: 11711750, with software. ACUSON Maple Select 1.0 Diagnostic Ultraso…

August 15, 2024 · Medical device recalls Moderate risk If ultrasound systems with software, are changed from factory default to : 1) M…

Siemens Medical Solutions USA, Inc. recalls ACUSON Juniper 1.0, 1.5, 2.0, 2.5 Diagnostic Ultrasound Systems, REF: 11335791, with software. ACUSON Juniper Select 2.…

August 15, 2024 · Medical device recalls Moderate risk If ultrasound systems with software, are changed from factory default to : 1) M…

Siemens Medical Solutions USA product recalled over injury risk

July 3, 2024 · Medical device recalls Moderate risk If the Sensis documentation functionality is used during adding of once-per-stu…

Siemens Medical Solutions USA product recalled over injury risk

July 3, 2024 · Medical device recalls Moderate risk If the Sensis documentation functionality is used during adding of once-per-stu…

Siemens Medical Solutions USA product recalled over injury risk

July 3, 2024 · Medical device recalls Moderate risk If the Sensis documentation functionality is used during adding of once-per-stu…

Siemens Medical Solutions USA product recalled over injury risk

July 3, 2024 · Medical device recalls Moderate risk If the Sensis documentation functionality is used during adding of once-per-stu…

Siemens Medical Solutions USA, Inc recalls Multitom Rax -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image Model Num…

July 2, 2024 · Medical device recalls Moderate risk The support arm may unintentionally lower resulting in injury to persons when t…

Siemens Medical Solutions USA, Inc recalls Luminos dRF Max- Intended to visualize anatomical structures by converting an x-ray pattern into a visible image. Model…

July 2, 2024 · Medical device recalls Moderate risk The support arm may unintentionally lower resulting in injury to persons when t…

Siemens Medical Solutions USA, Inc recalls Luminos Agile Max -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image. Mod…

July 2, 2024 · Medical device recalls Moderate risk The support arm may unintentionally lower resulting in injury to persons when t…

Siemens Medical Solutions USA, Inc recalls LUMINOS Lotus Max -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image Mode…

July 2, 2024 · Medical device recalls Moderate risk The support arm may unintentionally lower resulting in injury to persons when t…