Use cautionMedical device recall · FDA · Published December 16, 2022
Siemens ARTIS Pheno Biplane Recall: Table Connection May Detach
Siemens Medical recalls ARTIS pheno, icono biplane, and icono floor models due to risk of tabletop detachment. Affected units have specific material and UDI/DI numbers. Contact for repair or replacement.
“Siemens ARTIS Pheno Biplane Recall: Table Connection May Detach.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/59098-siemens-artis-pheno-biplane-recall-table-connection-may-detach. Based on FDA recall #Z-0956-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0956-2023%22&limit=1).
The FDA announced on 2022-12-16 that Siemens Medical Solutions USA, Inc. is recalling ARTIS pheno, ARTIS icono biplane, and ARTIS icono floor medical devices due to a potential loss of mechanical connection between the tabletop and table base.
How to tell if you have it
Siemens Medical ARTIS pheno (Material #10849000; UDI/DI: 4056869046877)
Siemens Medical ARTIS icono biplane (Material #11327600; UDI/DI: 4056869063317)
Siemens Medical ARTIS icono floor (Material #11327700; UDI/DI: 4056869149325)
The hazard
The mechanical connection between the tabletop and table base may be lost, according to the FDA.
Context
GovInfoNow's records show Siemens Medical Solutions USA, Inc. has had 182 other recalls since 2017-06-06. Recent similar recalls include the Siemens ARTIS icono Ceiling Monitor Recall on 2026-06-08 and the Siemens ARTIS icono floor recall on 2026-05-20. Other recent recalls of similar products include the Philips Azurion 7 B20 System Recall (2026-01-26), the Philips Azurion 7 M20 System Recall (2026-01-26), and the Philips Azurion 3 M15 System Recall (2026-01-26).
How to tell if you have this one
Check for the specific material numbers: 10849000 for ARTIS pheno, 11327600 for icono biplane, and 11327700 for icono floor. Also look for the UDI/DI numbers listed in the recall notice.
Brand
Siemens Medical
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Connection
Inspect the mechanical connection between the tabletop and table base for signs of looseness or damage.
Contact Manufacturer
Reach out to Siemens Medical Solutions USA, Inc for guidance on repair or replacement options.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Worldwide distribution - US Nationwide and the countries of Armenia, Australia, Austria, Belgium, Bulgaria, Canada, Chile, China, Colombia, Czech Republic, Denmark, Egypt, Finland, France, Germany, Greece, Hong Kong, India, Indonesia,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 40 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0956-2023 (December 16, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0956-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.