← FDA ENFORCEMENT
Z-2206-2026Class II

Siemens Medical Solutions USA, Inc

Recalling firm
Siemens Medical Solutions USA, Inc
Product type
Device
Status
Ongoing
Report date
2026-06-10
Distribution
US and Worldwide
Firm state
PA
Initiated by
FDA Mandated
Reason for recall

During patient examinations, the system may sporadically display a 0 x-ray dose administered to the patient. This behavior has only been observed during fluoroscopy and/or single-frame acquisitions. Despite the reported x-ray dose showing 0, an actual x-ray dose is applied to the patient.

Product description

ARTIS Icono biplane, floor and ceiling.: ARTIS icono biplane Model 11327600. ARTIS icono ceiling Model 11328100. ARTIS icono floor Model 11327700. interventional fluoroscopic x-ray system

Code / lot info

ARTIS icono biplane UDI 4056869063317 ARTIS icono ceiling UDI 4056869295923 ARTIS icono floor UDI 4056869149325

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.