PlainRecalls

Siemens Medical Solutions USA, Inc

Compiled from official public sources by the editorial team.

790 recalls on record · Latest: Apr 22, 2026

Siemens Medical Solutions USA, Inc Recall Insight

Siemens Medical Solutions USA, Inc appears on 790 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.777% 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 Apr 22, 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 Aug 12, 2020 to Dec 1, 2021.

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 Dec 1, 2021

Artis zee ceiling with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure …

FDA Devices Moderate Dec 1, 2021

SOMATOM Definition AS with software syngo.CT VB20 Model #8098027

FDA Devices Moderate Dec 1, 2021

Artis Q.zen biplane with software VD12- angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model …

FDA Devices Moderate Dec 1, 2021

Artis zee biplane with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Mo…

FDA Devices Moderate Dec 1, 2021

SOMATOM Force with software syngo.CT VB20 Model #10742326

FDA Devices Moderate Dec 1, 2021

SOMATOM Definition Flash with software syngo.CT VB20 Model #10430603

FDA Devices Moderate Dec 1, 2021

SOMATOM Confidence with software syngo.CT VB20 Model #10590100

FDA Devices Moderate Dec 1, 2021

Artis Q ceiling with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Mo…

FDA Devices Moderate Dec 1, 2021

SOMATOM Drive with software syngo.CT VB20 Model #10431700

FDA Devices Moderate Dec 1, 2021

SOMATOM Edge Plus with software syngo.CT VB20 Model #10267000

FDA Devices Moderate Dec 1, 2021

Artis Q.zen floor with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure M…

FDA Devices Moderate Dec 1, 2021

Artis zee multi-purpose with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure …

FDA Devices Moderate Nov 24, 2021

Sensis/ Sensis Vibe systems with software VD1X as follows: (1)Sensis Model 10764561 (2) Sensis Vibe Hemo Model 11007641 (3)Sensis Vibe Combo Model …

FDA Devices Moderate Nov 10, 2021

Artis zeego, Fluoroscopic X-Ray System Models: 10280959,10502505, 10848283 in combination with the following workplace/system application software m…

FDA Devices Moderate Sep 29, 2021

Computed tomography x-ray systems with software syngo.CT VA20A_SP4a, VA20A_SP5, VA30A_SP2, VA30A_SP2a, VA30A_SP3,VA30A_FP2 in Somatom systems: SOMAT…

FDA Devices Moderate Sep 22, 2021

syngo.CT VA20A, VA30A and VA40A in: syngo.via RT Image Suite / Sim&Go SOMATOM go.Now SOMATOM go.Up SOMATOM go.All SOMATOM go.Top SOMATOM…

FDA Devices Moderate Sep 22, 2021

syngo.via RT Image Suite with syngo.via VB30, VB40, VB50 and VB60- Intended for Radiation Therapy Treatment Material Number: 10496180

FDA Devices Moderate Sep 22, 2021

MR MAGNETOM Systems with RT Image Suite with syngo MR VA20A, VA30A and VA31A with license SW-Key CT_RT_IMA_SUITE_SYNTHETIC_CT Material Numbers: …

FDA Devices Moderate Sep 22, 2021

ACUSON Juniper Diagnostic Ultrasound System

FDA Devices Moderate Sep 8, 2021

Artis Models with SW version VD12 listed below: Artis zee floor 10094135 Artis zee ceiling 10094137 Artis zee MP 10094139 Artis Q floor 10848280 …

FDA Devices Moderate Jul 14, 2021

ARTIS pheno- angiography systems developed for single and biplane diagnostic imaging and interventional procedures. Model: 10849000

FDA Devices Moderate Jun 9, 2021

Multitom RAX with software version VF10

FDA Devices Moderate May 5, 2021

Artis systems - Product Usage: an angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, bu…

FDA Devices Moderate May 5, 2021

Interventional Fluoroscopic X-Ray System ARTIS icono biplane- 11327600 ARTIS icono floor- 11327700 ARTIS pheno- 10849000 ARTIS is a family of d…

FDA Devices Moderate May 5, 2021

Artis zee ceiling-interventional Fluoroscopic X-Ray System Model Number: 10094137

FDA Devices Moderate Apr 28, 2021

Sensis/ Sensis Vibe Hemo systems with VD12A software as follows: Dedicated SIS Server- 6648153 Sensis Post-Processing Workstation- 6648161 Sensi…

FDA Devices Moderate Apr 14, 2021

Ysio X.pree, Model Number: 11107464 - Product Usage: A Digital X-Ray System generate Xray images from the whole body including the skull, chest, abd…

FDA Devices Moderate Apr 7, 2021

Product Label - ACUSON Sequoia *** Power Input: 100-240V~, 13.0-5.4A, 50-60Hz *** (240)11148775 Model User Manual states - ACUSON Sequoia Diagnost…

FDA Devices Moderate Mar 31, 2021

Interventional Fluoroscopic X-Ray System - Product Usage: developed for single and biplane diagnostic imaging and interventional procedures including…

FDA Devices Moderate Mar 24, 2021

Software versions syngo.CT VA30A_SP2 or syngo.CT VA30A_SP2a in the Computed tomography systems as follows: SOMATOM go.Now (Model 11061610)SOMATOM …

FDA Devices Moderate Mar 10, 2021

Sensis / Sensis Vibe systems with software version VD12 and equipped with HP Flex Pro-C PC. Diagnostic and administrative tool supporting hemodynami…

FDA Devices Moderate Mar 3, 2021

ARTIS Icono biplane Model:11327600 ARTIS Icono floor system Model: 11327700 with software version VE20B - Product Usage: Intended for single and b…

FDA Devices Moderate Jan 20, 2021

SOMATOM Force, Definition AS, Definition Edge, Definition Flash, Drive, Confidence and Edge Plus

FDA Devices Moderate Jan 20, 2021

Artis zee/ zeego & Artis Q/ Q.zen Artis Pheno

FDA Devices Moderate Jan 20, 2021

Uroskop Omnia, Model no. 10094910 - Product Usage: a solid state detector fluoroscopic X-ray system, primarily for urological applications (functiona…

FDA Devices Moderate Jan 20, 2021

Uroskop Omnia Max, Model no. 10762473 - Product Usage: a solid state detector fluoroscopic X-ray system, primarily for urological applications (funct…

FDA Devices Moderate Nov 25, 2020

Artis zee floor, Artis Q ceiling, Artis Q.zen ceiling. Image-Intensified Fluoroscopic X-Ray System. Material numbers 10848281, 10848354, 10094135, 10…

FDA Devices Moderate Nov 11, 2020

ARTIS Icono Interventional Fluoroscopic X-Ray system - Product Usage: Intended Use: ARTIS is a family of dedicated angiography systems developed for …

FDA Devices Moderate Nov 4, 2020

Siemens Artis one systems with a Display Port transceiver-Fluoroscopic X-Ray System Model: 10848600 - Product Usage: he examination table as an inte…

FDA Devices Moderate Oct 21, 2020

Artis zee or Artis Q systems (listed below) - Product Usage: for single and biplane diagnostic imaging and interventional procedures. System Name/…

FDA Devices Moderate Oct 14, 2020

ACUSON AcuNav Volume Intracardiac Echocardiography Catheter 12.5F

FDA Devices Moderate Oct 7, 2020

Software versions syngo.CT VB20 or VB20_SP1 in the following systems: SOMATOM Force (Model #10742326) SOMATOM Definition As (Model #8098027) SOMAT…

FDA Devices Moderate Sep 30, 2020

Software: Syngo.via RT Image Suite software version VA30_SP02 with license T_RT_IMAGE_SUITE_PAT_MARK Intended Use: used as an advanced application o…

FDA Devices Moderate Sep 9, 2020

Symbia S-Series and Symbia T-Series - Product Usage: Intended use of the device SPECT: To detect or image the distribution of radionuclides in the …

FDA Devices Moderate Sep 9, 2020

Siemens Sensis Vibe Hemo system in combination with the MicroPodTM EtCO2 module-diagnostic and administrative tool supporting hemodynamic catheteriza…

FDA Devices Moderate Sep 2, 2020

Cios Spin, Image-Intensified Fluoroscopic X-Ray System The Cios Alpha and Cios Spin are a mobile X-Ray system designed to provide X-ray imaging of…

FDA Devices Moderate Sep 2, 2020

E.cam or Symbia systems that use foresight detectors - Product Usage: To detect or image the distribution of radionuclides in the body or organ, usin…

FDA Devices Moderate Sep 2, 2020

Cios Alpha (VA20) - Model: 10308191 Cios Alpha (VA30) - Model: 11105200 Cios Spin (VA30) - Model: 10308194 Cios Alpha and Cios Spin are a mobil…

FDA Devices Moderate Sep 2, 2020

Cios Alpha, Image-Intensified Fluoroscopic X-Ray System The Cios Alpha and Cios Spin are a mobile X-Ray system designed to provide X-ray imaging o…

FDA Devices Moderate Aug 12, 2020

SIEMENS Healthineers Uroskop Omnia max Model: 10762473 - Product Usage: is a device intended to visualize anatomical structures by converting an X-…

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Siemens Medical Solutions USA, Inc with Zimmer Biomet, Inc. →

Data Sources

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

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.