PlainRecalls

Siemens Medical Solutions USA, Inc

525 recalls on record · Latest: Feb 11, 2026

Siemens Medical Solutions USA, Inc Recall Insight

Siemens Medical Solutions USA, Inc appears on 525 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.625% of the federal archive — a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Feb 11, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 0 critical, 50 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 entries — unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Mar 29, 2017 to May 16, 2018.

Manufacturer-level browsing is useful when monitoring a single firm for patterns — whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current — deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement — always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate May 16, 2018

Syngo.plaza software Syngo.Plaza is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate…

FDA Devices Moderate May 16, 2018

Syngo.Via VB20A model 1049610

FDA Devices Moderate May 9, 2018

SOMATOM Spirit Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data.

FDA Devices Moderate May 9, 2018

SOMATOM Sensation Open Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data.

FDA Devices Moderate May 9, 2018

SOMATOM Scope Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data.

FDA Devices Moderate May 9, 2018

SOMATOM Sensation 64 Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data.

FDA Devices Moderate May 9, 2018

SOMATOM Emotion (2003) Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data.

FDA Devices Moderate May 9, 2018

SOMATOM Perspective Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data.

FDA Devices Moderate May 9, 2018

Biograph Horizon - PET/CT, PETsyngo VJ20A Software Nuclear medicine/ xray diagnostic scanner.

FDA Devices Moderate May 9, 2018

SOMATOM Sensation 40 Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data.

FDA Devices Moderate May 9, 2018

SOMATOM Sensation Cardiac Intended to produce cross-sections images of the body by computer reconstruction of x-ray transmission data.

FDA Devices Moderate Apr 25, 2018

PRIMUS HI, Digital Linear Accelerator, Model No. 04504200 Product Usage: The intended use of the device is to deliver x-ray radiation for therape…

FDA Devices Moderate Apr 25, 2018

MEVATRON M2 / PRIMUS Mid-Energy, Digital Linear Accelerator, Model No. 01940035 Product Usage: The intended use of the device is to deliver x-ray…

FDA Devices Moderate Apr 25, 2018

ONCOR Impression , Digital Linear Accelerator, Model No. 05857920 Product Usage: The intended use of the device is to deliver x-ray radiation for…

FDA Devices Moderate Apr 4, 2018

Syngo.via software is intended to be used for viewing, manipulation, communication, and storage of medical images. It can be used as a standalone dev…

FDA Devices Moderate Mar 28, 2018

Artis one fluoroscopic x-ray system and patient table Artis one is an angiography system developed for diagnostic imaging and interventional pro…

FDA Devices Moderate Mar 28, 2018

AXIOM Artis angiographic x-ray system, Model Numbers: 7412807, 7413078, 7728392 AXIOM Artis is a family of dedicated angiography systems develope…

FDA Devices Moderate Mar 7, 2018

Axiom Artis, Model Numbers: 5904433, 5904441, 5904649, 5904656, 5917054, 7007755, 7008605, 7412807, 7413078, 7555357, 7555373, 7727717, 7728350 & 772…

FDA Devices Moderate Mar 7, 2018

Artis Q and Q.zen model Interventional fluoroscopic x-ray system wireless foot switch accessory; Model Numbers: 4787797, 4787805, and 4787813.

FDA Devices Moderate Mar 7, 2018

SOMATOM Go.Up computed tomography (CT) x-ray system table, Model Number: 11061628 Product Usage: Intended to generate and process cross-sectional…

FDA Devices Moderate Mar 7, 2018

Artis zee and Artis zeego model Interventional fluoroscopic x-ray foot switch accessory; Model Numbers: 4787797, 4787805, and 4787813.

FDA Devices Moderate Mar 7, 2018

SOMATOM Go.Now computed tomography (CT) x-ray system table, Model Number: 11061618 Product Usage: Intended to generate and process cross-sectiona…

FDA Devices Moderate Feb 14, 2018

AArtis Q/ Q.Zen biplane Artis zee biplane Product Usage: Artis is a family of dedicated angiography systems developed for single and biplane diagno…

FDA Devices Moderate Feb 14, 2018

Syngo.plaza systems with SW VB20A, Model Number - 10863171, 10863172, 10863173 Product Usage: Syngo.plaza is a Picture Archiving and Communicatio…

FDA Devices Moderate Feb 7, 2018

Syngo.plaza Picture Archiving and Communication System (PACS) with software version VB20A; Model numbers: 10863171, 10863172, 10863173 Syngo.plaza…

FDA Devices Moderate Jan 31, 2018

Syngo Imaging version V31 (model # 10014063) is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, commu…

FDA Devices Moderate Nov 29, 2017

Syngo.plaza, Picture Archiving and Communications System(PACS), Model 10863171 Syngo.plaza is a Picture Archiving and Communication System (PACS…

FDA Devices Moderate Nov 22, 2017

Symbia Intevo 16, SPECT/CT System, Emission Computed Tomography System To detect or image the distribution of radionuclides in the body or organ, us…

FDA Devices Moderate Nov 22, 2017

Symbia Intevo 6, SPECT/CT System, Emission Computed Tomography System To detect or image the distribution of radionuclides in the body or organ, usi…

FDA Devices Moderate Nov 1, 2017

Torque wrench used on the bolts for the Symbia T2 model 10275008, Symbia Intevo Excel model 10764801, Symbia Intevo 16 model 10764804, Symbia Evo mod…

FDA Devices Moderate Sep 6, 2017

Artis zee/zeego and Artis Q/Q.zen system, x-ray, angiographic AXIOM Artis zee and Q/Q.zen is a family of dedicated angiography systems developed fo…

FDA Devices Moderate Sep 6, 2017

Artis zee/zeego and Artis Q/Q.zen system, x-ray, angiographic AXIOM Artis zee and Q/Q.zen is a family of dedicated angiography systems developed fo…

FDA Devices Moderate Sep 6, 2017

Artis zee/zeego and Artis Q/Q.zen system, x-ray, angiographic AXIOM Artis zee and Q/Q.zen is a family of dedicated angiography systems developed fo…

FDA Devices Moderate Sep 6, 2017

Artis zee/zeego and Artis Q/Q.zen system, x-ray, angiographic AXIOM Artis zee and Q/Q.zen is a family of dedicated angiography systems developed fo…

FDA Devices Moderate Sep 6, 2017

Artis zee/zeego and Artis Q/Q.zen system, x-ray, angiographic AXIOM Artis zee and Q/Q.zen is a family of dedicated angiography systems developed fo…

FDA Devices Moderate Sep 6, 2017

Artis zee/zeego and Artis Q/Q.zen system, x-ray, angiographic AXIOM Artis zee and Q/Q.zen is a family of dedicated angiography systems developed fo…

FDA Devices Moderate Sep 6, 2017

Artis zee/zeego and Artis Q/Q.zen system, x-ray, angiographic AXIOM Artis zee and Q/Q.zen is a family of dedicated angiography systems developed fo…

FDA Devices Moderate Sep 6, 2017

Artis zee/zeego and Artis Q/Q.zen system, x-ray, angiographic AXIOM Artis zee and Q/Q.zen is a family of dedicated angiography systems developed fo…

FDA Devices Moderate Sep 6, 2017

Artis zee/zeego and Artis Q/Q.zen system, x-ray, angiographic AXIOM Artis zee and Q/Q.zen is a family of dedicated angiography systems developed fo…

FDA Devices Moderate Jul 12, 2017

Sensis Vibe Systems with Software Version VD10B, Model Numbers 10765502, 10910620, 11007641, 6648161 --- Programmable diagnostic computer,

FDA Devices Moderate May 31, 2017

AXIOM Sensis, Computer, Diagnostic, Programmable. Intended to be used as a diagnostic and administrative tool supporting hemodynamic cardiac cathe…

FDA Devices Moderate May 3, 2017

18L6 HD transducer on the ACUSON S Family ultrasound systems with software versions VD10A or VD10C; Model numbers: 18L6 HD transducer  10041227 …

FDA Devices Moderate Apr 26, 2017

Artis zee, Angiographic x-ray system

FDA Devices Moderate Apr 19, 2017

Combi Dockable Neurosurgery table for the Siemens MAGNETOM Aera (1.5T) and Skyra (3T) MRI Systems

FDA Devices Moderate Apr 5, 2017

Syngo.x, Picture archiving and communication system Syngo via is a software solution intended to be used for viewing, manipulation, communication, a…

FDA Devices Moderate Mar 29, 2017

ONCOR" Avant-garde

FDA Devices Moderate Mar 29, 2017

ONCOR" Expression ONCOR" Impression ONCOR" Impression plus

FDA Devices Moderate Mar 29, 2017

ARTIS Q, Interventional Fluroscopic x-ray system

FDA Devices Moderate Mar 29, 2017

Syngo.plaza, Picture Archiving and Communications System (PACS) Syngo.plaza is a Picture Archiving and Communication System (PACS) intended to displ…

FDA Devices Moderate Mar 29, 2017

Mevatron M2/Primus Mid-Energy PRIMUS HI

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Siemens Medical Solutions USA, Inc with FORD →

Data Sources

  • Source: FDA + CPSC + NHTSA + USDA FSIS — federal recall filings naming this firm. Verify with FDA, CPSC, NHTSA, or USDA FSIS directly.
  • Source: PlainRecalls Manufacturer Index — firm-level aggregation across all four federal recall feeds