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 Jul 10, 2019 to Nov 20, 2019.

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 Nov 20, 2019

Software versions syngo CT VB20 running on the following Siemens SOMATOM CT Scanner. SOMATOM Force (Model #10742326), SOMATOM Definition As (Model…

FDA Devices Moderate Oct 30, 2019

Mammomat Revelation with software version VC10 and Biopsy Option Intended Use: For mammography exams, screening, diagnostics, biopsies and dual en…

FDA Devices Moderate Sep 11, 2019

syngo.CT software version VA48A_SP5.5 in the following SOMATOM computed tomography models: SOMATOM Definition Edge-Model #10590000; SOMATOM Definit…

FDA Devices Moderate Sep 4, 2019

SOMATOM go.Top; Models #11061640 Product Usage: This computed tomography system is intended to generate and process cross-sectional images of p…

FDA Devices Moderate Sep 4, 2019

SOMATOM go.Top; Models #11061648 Product Usage: This computed tomography system is intended to generate and process cross-sectional images of p…

FDA Devices Moderate Sep 4, 2019

SOMATOM go.Now; Models #11061610 & 11061618 Product Usage: This computed tomography system is intended to generate and process cross-sectional …

FDA Devices Moderate Sep 4, 2019

SOMATOM go.All; Models #11061638 Product Usage: This computed tomography system is intended to generate and process cross-sectional images of p…

FDA Devices Moderate Aug 28, 2019

ACUSON NX2 Elite Diagnostic Ultrasound System, Model # 11284500, RX Only, Siemens Medical Solutions, containing software version VA10A, VA10B, VA11A…

FDA Devices Moderate Aug 28, 2019

MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643

FDA Devices Moderate Aug 28, 2019

ACUSON NX3 Diagnostic Ultrasound System, Model # 11235612, RX Only, Siemens Medical Solutions, containing software versions: VA10A, VA10B, VA10C, V…

FDA Devices Moderate Aug 28, 2019

MAGNETOM Prisma magnetic resonance diagnostic devices Model #10849582

FDA Devices Moderate Aug 28, 2019

ACUSON NX3 Elite Diagnostic Ultrasound System, Model # 11235411, RX Only, Siemens Medical Solutions, containing software versions: VA10A, VA10B, VA…

FDA Devices Moderate Aug 28, 2019

ACUSON NX2 Diagnostic Ultrasound System, Model # 11284381, RX Only, Siemens Medical Solutions, containing software version VA10A, VA10B, VA11A, VA11…

FDA Devices Moderate Aug 28, 2019

MAGNETOM Skyra magnetic resonance diagnostic devices Model # 10432915

FDA Devices Moderate Aug 28, 2019

MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914

FDA Devices Moderate Aug 21, 2019

SOMATOM Definition AS, Model Number 8098027 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of p…

FDA Devices Moderate Aug 21, 2019

SOMATOM Drive, Model Number 10431700 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients…

FDA Devices Moderate Aug 21, 2019

SOMATOM Force, Model Number 10742326 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients…

FDA Devices Moderate Aug 21, 2019

SOMATOM Edge Plus, Model Number 10267000 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of pati…

FDA Devices Moderate Aug 21, 2019

SOMATOM Definition Edge, Model Number 10590000 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images o…

FDA Devices Moderate Aug 21, 2019

SOMATOM Definition Flash, Model Number 10430603 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images …

FDA Devices Moderate Aug 14, 2019

Lantis Commander, Model # 4503178 - Product Usage: Lantis Treatstation is to allow the radiation therapist to deliver treatment to the patient usin…

FDA Devices Moderate Aug 14, 2019

Lantis 8.3 Commander, Model # 8148178 - Product Usage: Lantis Treatstation is to allow the radiation therapist to deliver treatment to the patient us…

FDA Devices Moderate Jul 31, 2019

AXIOM Artis dTC, Model Number 7413078

FDA Devices Moderate Jul 31, 2019

AXIOM Artis FA, Model Number 5904441

FDA Devices Moderate Jul 31, 2019

Artis zee floor MN, Model Number 10094142

FDA Devices Moderate Jul 31, 2019

AXIOM Artis dMP, Model Number 7555365

FDA Devices Moderate Jul 31, 2019

AXIOM Artis dBC, Model Number 7728392

FDA Devices Moderate Jul 31, 2019

Artis zee ceiling, Model Number 10094137

FDA Devices Moderate Jul 31, 2019

AXIOM Artis dBA, Model Number 7555357

FDA Devices Moderate Jul 31, 2019

AXIOM Artis dFA, Model Number 7555373

FDA Devices Moderate Jul 31, 2019

Artis zee floor, Model Number 10094135

FDA Devices Moderate Jul 31, 2019

AXIOM Artis dTA, Model Number 7008605

FDA Devices Moderate Jul 31, 2019

Artis zee biplane, Model Number 10094141

FDA Devices Moderate Jul 31, 2019

Artis zeego, Model Number 10280959

FDA Devices Moderate Jul 31, 2019

Artis zee multi, Model Number 10094139

FDA Devices Moderate Jul 31, 2019

AXIOM Artis TA, Model Number 7007755

FDA Devices Moderate Jul 31, 2019

AXIOM Artis dFC, Model Number 7727717

FDA Devices Moderate Jul 31, 2019

AXIOM Artis BA, Model Number 5904656

FDA Devices Moderate Jul 17, 2019

Cios care fusion system

FDA Devices Moderate Jul 17, 2019

Cios Alpha VA20/ VA30 mobile X-Ray systems

FDA Devices Moderate Jul 10, 2019

SOMATOM go.Up (Model #11061610) with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is intende…

FDA Devices Moderate Jul 10, 2019

SOMATOM go.Now, Model No. 11061618 with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is …

FDA Devices Moderate Jul 10, 2019

Siemens Artis zee floor -Interventional Fluoroscopic X-Ray System Model Number: 10094135

FDA Devices Moderate Jul 10, 2019

SOMATOM go.Top, Model No. 11061648 with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is …

FDA Devices Moderate Jul 10, 2019

Siemens Artis Q zeego ---Interventional Fluoroscopic X-Ray System Model Number: 10848283

FDA Devices Moderate Jul 10, 2019

Siemens Artis Q floor --Interventional Fluoroscopic X-Ray System Model Number: 10848280

FDA Devices Moderate Jul 10, 2019

Siemens Artis Q ceiling--Interventional Fluoroscopic X-Ray System Model Number: 10848281

FDA Devices Moderate Jul 10, 2019

SOMATOM go.All (Model #11061630), with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is inte…

FDA Devices Moderate Jul 10, 2019

Siemens Artis zee biplane-Interventional Fluoroscopic X-Ray System Model Number: 10094141

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