ProductGuru Recalls

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Siemens Medical Solutions USA, Inc: official recall notices

23 official recall or safety notices on this site name Siemens Medical Solutions USA, Inc, dated between 2024-02-23 and 2026-03-12. They were issued by 1 authority: US FDA — Medical Devices (23).

Countries where the notices were issued: United States (22), Germany (1).

Name as written in the notices: Siemens Medical Solutions USA, Inc; Siemens Medical Solutions USA, Inc.; SIEMENS MEDICAL SOLUTIONS USA, INC. This is the brand or the responsible company as each authority recorded it. A recall shows a safety system working; it is not a verdict on a brand. Follow the official notice for each product.

Notices by year

YearNotices
20264
202513
20246

Notices by authority

AuthorityNotices
US FDA — Medical Devices23

All notices

DateAuthorityProductHazard (as classified)
2026-03-12US FDA — Medical DevicesARTIS Pheno VE30A and VE40A, Model 10849000—
2026-03-10US FDA — Medical DevicesARTIS pheno and ARTIS Icono biplane, floor and ceiling. Model Numbers 10849000, 11327600, 11328100, 11327700.—
2026-03-09US FDA — Medical DevicesARTIS Icono biplane, floor and ceiling.: ARTIS icono biplane Model 11327600. ARTIS icono ceiling Model 11328100. ARTIS i—
2026-03-09US FDA — Medical DevicesARTIS pheno, Model 10849000. interventional fluoroscopic x-ray system—
2025-12-05US FDA — Medical DevicesLUMINOS Lotus Max, Model 11574100 and Luminos dRF Max, Model 10762471—
2025-08-28US FDA — Medical DevicesMAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347, K111242, K123510, K133435, K140253, K141977, K1—
2025-08-28US FDA — Medical DevicesBiograph mMR. Model Number: 10433372.—
2025-08-28US FDA — Medical DevicesMAGNETOM Verio. Model Number: 10276755.—
2025-08-28US FDA — Medical DevicesMAGNETOM Lumina (DE). Model Number: 11344916.—
2025-08-28US FDA — Medical DevicesMAGNETOM Spectra as the following: 1. MAGNETOM Spectra. Model Number: 10837643. 2. MAGNETOM Spectra (CN). Model Numbe—
2025-08-28US FDA — Medical DevicesMAGNETOM Skyra Fit BioMatrix. Model Number: 11516217.—
2025-08-28US FDA — Medical DevicesMAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396, K173617, K181433, K183254, K192924, K203443, K213693,—
2025-08-28US FDA — Medical DevicesMAGNETOM Vida Fit. Model Number: 11410481.—
2025-08-28US FDA — Medical DevicesMAGNETOM Skyra fit. Model Number: 10849580.—
2025-08-28US FDA — Medical DevicesMAGNETOM Cima.X (DE). Model Number: 11647158.—
2025-08-28US FDA — Medical DevicesMAGNETOM Verio Dot Upgrade. Model Number: 10684334.—
2025-01-02US FDA — Medical DevicesARTIS One Angiographic X-Ray System—
2024-08-15US FDA — Medical DevicesACUSON Juniper 1.0, 1.5, 2.0, 2.5 Diagnostic Ultrasound Systems, REF: 11335791, with software. ACUSON Juniper Select 2.—
2024-08-15US FDA — Medical DevicesACUSON Maple 1.0 Diagnostic Ultrasound System, REF: 11711750, with software. ACUSON Maple Select 1.0 Diagnostic Ultraso—
2024-08-15US FDA — Medical DevicesACUSON Redwood 1.0 and 2.0 Diagnostic Ultrasound Systems, REF: 11503314, with software—
2024-03-21US FDA — Medical DevicesSiemens Artis Models: Interventional Fluoroscopic X-Ray Systems-Models: Artis zee floor- 10094135 Artis zee ceiling- 1—
2024-02-23US FDA — Medical DevicesACUSON Redwood 1.0 Diagnostic Ultrasound System, REF: 11503314, running software version VA10A to VA10G—
2024-02-23US FDA — Medical DevicesACUSON Maple Diagnostic Ultrasound System, REF: 11711750, ACUSON Maple Select, REF: 11711779, running software version V—

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