Siemens Medical Solutions USA, Inc
796 recalls on record · Latest: Jul 8, 2026
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Agency notice ledger
Federal filing book Siemens Medical Solutions U… HEAVY-BOOK · SINGLE-AGENCY
#3 of 14,151 · 796 notices · 0.762% archive
- BOOK 796 notices
- RANK #3 of 14,151
- SHARE 0.762% archive
- AGENCY FDA Devices (796)
- CAT medical devices
- CATS 1 category
- LATEST Jul 8, 2026
- PHOTO Ford
Nearest notice-volume peer: Ford (14 notice gap)
Siemens Medical Solutions USA, Inc sits #3 of 14,151 (3rd among 14,151 firms) with 796 federal notices — about 0.762% of the archive (heavy-book tercile). Rank counts issuance frequency, not danger. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →
Siemens Medical Solutions U…'s standing among 14,151 recalling firms
Siemens Medical Solutions USA, Inc ranks 3rd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.
Siemens Medical Solutions U… vs all firms by recall-notice count
Where this firm's archive sits among every tracked recalling manufacturer
796 3rd of 14151 higher than 14,148 of 14,151 firms
Firms, banded by distinct federal recall-event inventory
Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-14
Siemens Medical Solutions U… in the notice-volume neighbourhood
Distinct federal recall events among this firm and nearest nationwide peers
- Zimmer Biomet…
Zimmer Biomet, Inc.
875 notices
- Medline Indus…
Medline Industries, LP - Northfield
822 notices
- Siemens Medic… (this)
Siemens Medical Solutions USA, Inc
796 notices
- Ford
Ford
782 notices
- Customed, Inc
Customed, Inc
682 notices
- Siemens Healt…
Siemens Healthcare Diagnostics, Inc.
665 notices
What this shows Siemens Medical Solutions USA, Inc carries 796 distinct federal notices, ranked #3 of 14,151 (heavy-book).
FDA Devices Moderate Sep 4, 2019
SOMATOM go.All; Models #11061630 Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data
FDA Devices Moderate Sep 4, 2019
Artis zee and Artis Q/ Q.zen Interventional Fluoroscopic X-Ray System with patient tables as follows: Systems Material Number Artis zee biplane 10094141; Artis Q floor 10848280; Artis Q biplane 10848282; Artis Q.zen floor 10848353; Artis Q.zen biplane 10848355; Artis zee ceiling 10094137; Artis Q ceiling 10848281; Artis Q zeego 10848283 ArtisQ.zen ceiling 10848354 Product Usage: Artis is a family of dedic
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, VA11B; UDI # 04056869050775 The ACUSON NX2 diagnostic ultrasound imaging systems are intended for the following applications: Cardiac, Fetal, Abdominal (including liver), Pediatric, Small Parts (Small Organ), Transcranial, OB/GYN, Pelvic, Urology, Vascular (including Peripheral Vessel) and Musculoskeletal applications. The systems also provide
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, VA10D, VA10E, VA10F, VB20A, and VB20B; UDI # 04056869004297 The ACUSON NX2 diagnostic ultrasound imaging systems are intended for the following applications: Cardiac, Fetal, Abdominal (including liver), Pediatric, Small Parts (Small Organ), Transcranial, OB/GYN, Pelvic, Urology, Vascular (including Peripheral Vessel) and Musculoskeletal applica
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, VA10C, VA10D, VA10E, VA10F, VB20A, and VB20B; UDI # 04056869004303 The ACUSON NX2 diagnostic ultrasound imaging systems are intended for the following applications: Cardiac, Fetal, Abdominal (including liver), Pediatric, Small Parts (Small Organ), Transcranial, OB/GYN, Pelvic, Urology, Vascular (including Peripheral Vessel) and Musculoskeletal a
FDA Devices Moderate Aug 28, 2019
ACUSON NX2 Diagnostic Ultrasound System, Model # 11284381, RX Only, Siemens Medical Solutions, containing software version VA10A, VA10B, VA11A, VA11B; UDI # 04056869030005 The ACUSON NX2 diagnostic ultrasound imaging systems are intended for the following applications: Cardiac, Fetal, Abdominal (including liver), Pediatric, Small Parts (Small Organ), Transcranial, OB/GYN, Pelvic, Urology, Vascular (including Peripheral Vessel) and Musculoskeletal applications. The systems also provide for t
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 patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician as an aid in diagnosis. The images delivered by the system can be used by trained staff as an aid in diagnosis, treatment preparation and radiation therapy planning. These CT systems can be used for low dose lunch canc
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 by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician as an aid in diagnosis. The images delivered by the system can be used by trained staff as an aid in diagnosis, treatment preparation and radiation therapy planning. These CT systems can be used for low dose lunch cancer scre
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 by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician as an aid in diagnosis. The images delivered by the system can be used by trained staff as an aid in diagnosis, treatment preparation and radiation therapy planning. These CT systems can be used for low dose lunch cancer scre
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 patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician as an aid in diagnosis. The images delivered by the system can be used by trained staff as an aid in diagnosis, treatment preparation and radiation therapy planning. These CT systems can be used for low dose lunch cancer
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 of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician as an aid in diagnosis. The images delivered by the system can be used by trained staff as an aid in diagnosis, treatment preparation and radiation therapy planning. These CT systems can be used for low dose lunch c
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 of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician as an aid in diagnosis. The images delivered by the system can be used by trained staff as an aid in diagnosis, treatment preparation and radiation therapy planning. These CT systems can be used for low dose lunch
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 patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician as an aid in diagnosis. The images delivered by the system can be used by trained staff as an aid in diagnosis, treatment preparation and radiation therapy planning. These CT systems can be used for low dose lunch cancer
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 using the mevatron and all available accessories. This entails selecting a patient, selecting today s treatment for that patient, setting up and delivering the treatment fields and recording the delivered treatment. Treatstation supports auto sequencing, a process of automatically downloading a group of fields or segments from the verification and recor
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 using the mevatron and all available accessories. This entails selecting a patient, selecting today s treatment for that patient, setting up and delivering the treatment fields and recording the delivered treatment. Treatstation supports auto sequencing, a process of automatically downloading a group of fields or segments from the verification and rec
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 using the mevatron and all available accessories. This entails selecting a patient, selecting today s treatment for that patient, setting up and delivering the treatment fields and recording the delivered treatment. Treatstation supports auto sequencing, a process of automatically downloading a group of fields or segments from the verification and rec
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 using the mevatron and all available accessories. This entails selecting a patient, selecting today s treatment for that patient, setting up and delivering the treatment fields and recording the delivered treatment. Treatstation supports auto sequencing, a process of automatically downloading a group of fields or segments from the verification and
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 intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician as an aid in diagnosis. The images delivered by the system can be used by trained staff as an aid in diagnosis, treatment preparation and radiation therapy planning.
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 intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician as an aid in diagnosis. The images delivered by the system can be used by trained staff as an aid in diagnosis, treatment preparation and radiation therapy pl
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 intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician as an aid in diagnosis. The images delivered by the system can be used by trained staff as an aid in diagnosis, treatment preparation and radiation therapy pl
Siemens Medical Solutions U… sits in the heavy federal notice book
Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.
Similar recall count
Nearest multi-notice firms by distinct-event totals (796 here — heavy-book).
Similar medical devices volume
Nearest multi-notice firms in the same narrow category lane.
Frequently Asked Questions
How many federal recall notices name Siemens Medical Solutions U…? ▼
PlainRecalls indexes 796 distinct federal recall events naming Siemens Medical Solutions USA, Inc, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Siemens Medical Solutions U… sit among other recalling firms? ▼
Siemens Medical Solutions USA, Inc ranks #3 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Siemens Medical Solutions U…'s notices? ▼
FDA Devices accounts for 796 of this firm's 796 indexed notices.
What product category dominates Siemens Medical Solutions U…'s filing book? ▼
Filings for Siemens Medical Solutions USA, Inc span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Siemens Medical Solutions USA, Inc: 796 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.
Firm-level totals aggregate distinct federal recall events naming Siemens Medical Solutions USA, Inc; individual notices remain authoritative on each linked recall page.
Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026