company
Siemens Medical Solutions USA, Inc
Jurisdiction: US
FDA Warning Letter timeline
V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.
- fda_recall · device_recall2026-06-10Siemens Medical Solutions USA, Inc — Class II recall: ARTIS pheno, Model 10849000. interventional fluoroscopic x-ray system
- fda_recall · device_recall2026-06-10Siemens Medical Solutions USA, Inc — Class II recall: ARTIS Icono biplane, floor and ceiling.: ARTIS icono biplane Model 11327600. ART…
- fda_recall · device_recall2026-04-22Siemens Medical Solutions USA, Inc — Class II recall: ARTIS Pheno VE30A and VE40A, Model 10849000
- fda_recall · device_recall2026-04-15Siemens Medical Solutions USA, Inc — Class II recall: ARTIS pheno and ARTIS Icono biplane, floor and ceiling. Model Numbers 10849000,…
Frequently asked questions
- How many FDA warning letters has Siemens Medical Solutions USA, Inc received?
- Argus HQ has not recorded an FDA warning letter for Siemens Medical Solutions USA, Inc in our current dataset.
- What FDA recalls has Siemens Medical Solutions USA, Inc issued?
- Argus HQ has recorded 4 FDA recalls tied to Siemens Medical Solutions USA, Inc.
- Is Siemens Medical Solutions USA, Inc FDA compliant?
- Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 4 recalls, and 0 approval records for Siemens Medical Solutions USA, Inc. Review the linked FDA source records directly before drawing a compliance conclusion.
Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.