Lower riskMedical device recall · FDA · Published February 25, 2022
Siemens Artis Icono Floor Recall: Software Issues May Delay Treatment
Siemens recalls Artis Icono floor systems with certain Siemens Healthineers or Trumpf/MAQUET tables due to potential software errors that may delay clinical treatment. Affected units have specific serial numbers and model codes.
Five potential software issues affecting Artis pheno and Artis icono systems in combination with a Siemens Healthineers table or Trumpf/MAQUET table (OEM). The potential software errors are related to the block movement s function and manual rotation of the flat detector. Depending on the status of the intervention, the limited functionality may not be sufficient to continue with treatment as planned. This may result in a situation where clinical treatment may be delayed until an additional restart is performed
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Contact the company
📍Recalling firmSiemens Medical Solutions USA, Inc40 Liberty Blvd · Malvern, PA 19355-1418
✎ GovInfoNow plain-language explainer
Siemens is recalling Artis Icono floor systems that work with specific Siemens Healthineers or Trumpf/MAQUET tables because software issues could cause treatment delays. This affects medical imaging equipment used for procedures requiring precise movement and rotation of the imaging detector. Read more at govinfonow.com/recall/61025-siemens-artis-icono-floor-recall-software-issues-may-delay-treatment.
“Siemens Artis Icono Floor Recall: Software Issues May Delay Treatment.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61025-siemens-artis-icono-floor-recall-software-issues-may-delay-treatment. Based on FDA recall #Z-0986-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0986-2022%22&limit=1).
The FDA announced on Feb. 25, 2022, that Siemens Medical Solutions USA, Inc. is recalling Artis icono floor systems combined with specific tables due to potential software issues. The agency stated the recall involves 35 units distributed nationwide.
How to tell if you have it
Brand: Siemens
Product: Artis icono floor in combination with a Siemens Healthineers table or Trumpf/MAQUET table (OEM)
According to the FDA, five potential software issues affect the block movement's function and manual rotation of the flat detector. These errors may limit functionality sufficiently to prevent continuation of planned treatment, potentially delaying clinical treatment until an additional restart is performed.
Context
GovInfoNow's records show Siemens Medical Solutions USA, Inc. has had 182 other recalls on record since June 6, 2017. Other recent recalls of similar products include Siemens ARTIS icono Ceiling Monitor Recall (June 8, 2026), Siemens ARTIS icono ceiling recall (May 20, 2026), and Siemens ARTIS Pheno VE30A/VE40A recall (March 12, 2026). Other recent recalls of similar products include Philips Achieva 3.0T MRI Recall (Aug. 21, 2026), Philips Azurion 5 M12 System Software Recall (Jan. 26, 2026), and Philips PIC iX Essentials Software Freeze recall (July 31, 2026).
How to tell if you have this one
Check for the Artis Icono floor system with Siemens Healthineers or Trumpf/MAQUET tables. Affected units have specific serial numbers listed in the recall notice, including model 11327700 and serial numbers starting with 170023 through 170378.
Brand
Siemens
Category
Medical device
FDA recall event · 3 products
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Artis icono floor in combination with a Siemens Healthineers table or Trumpf/MAQUET table (OEM). Intended use single and biplane diagnostic imaging and interventional procedures. Model: 11327700; S/N: Serial 170319 170026 170343 170367 170368 170305 170360 170307 170331 170349 170309 170310 170361 170351 170383 170023 170304 170328 170334 170336 170025 170346 170051 170358 170357 170333 170365 170332 170312 170027 170303 170378 170322 170053 170364 UDI: 04056869149325
35 units
Z-0987-2022
Artis pheno- in combination with a Siemens Healthineers table or Trumpf/MAQUET table (OEM). Intended use-single and biplane diagnostic imaging and interventional procedures. Model: 10849000; Serial Number: 164719 164712 164740 164722 164763 164735 164723 164743 164741 164728 164711 164718 164739 164703 164721 164726 164724 164725 164760 UDI: 04056869046877
20 units
Based on the official FDA remedy
What to do — step by step
Check System Details
Identify if your Artis Icono floor system is paired with a Siemens Healthineers or Trumpf/MAQUET table using the serial numbers listed in the recall notice.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 2 months 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.
No, the recall does not require immediate discontinuation. The hazard may cause treatment delays but does not pose an immediate risk of serious injury.
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-0986-2022 (February 25, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0986-2022 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.