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 Jul 10, 2019 to Aug 28, 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 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 21, 2019

SOMATOM Confidence, Model Number 10590100 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of pat…

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 Aug 14, 2019

Lantis 6.1 Commander, Model # 5493072 - Product Usage: Lantis Treatstation is to allow the radiation therapist to deliver treatment to the patient us…

FDA Devices Moderate Aug 14, 2019

Lantis system (pre-2003), Model #5835991 - Product Usage: Lantis Treatstation is to allow the radiation therapist to deliver treatment to the patient…

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 31, 2019

AXIOM Artis BC, Model Number 5904649

FDA Devices Moderate Jul 31, 2019

AXIOM Artis FC, Model Number 5904433

FDA Devices Moderate Jul 31, 2019

AXIOM Artis dBC, Model Number 5917054

FDA Devices Moderate Jul 31, 2019

AXIOM Artis MP, Model Number 5904466

FDA Devices Moderate Jul 31, 2019

AXIOM Artis TC, Model Number 7728350

FDA Devices Moderate Jul 31, 2019

AXIOM Artis dFC, Model Number 7412807

FDA Devices Moderate Jul 31, 2019

Artis zee biplane MN, Model Number 10094143

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

FDA Devices Moderate Jul 10, 2019

SOMATOM go.Top (Model #1161640), with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is inten…

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.