Siemens Medical Solutions Usa, Inc: Interventional Fluoroscopic X-ray System

Recalling firm
Siemens Medical Solutions USA, Inc
Product
ARTIS pheno, Model 10849000. interventional fluoroscopic x-ray system
Reason
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.
Classification
Class II
Category
medical device recall
Country
United States
Agency
FDA-DEVICES
Recall date
2026-03-09
Status
Open, Classified
Distribution
US and Worldwide

Official recall notice from FDA-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/94f3f1c4-c0aa-48b5-a875-be58fd072adc