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FDA device recallVulnerabilitiesPublished January 8, 2026

Siemens Medical Solutions USA, Inc: Interventional Fluoroscopic X-Ray System

A potential issue associated with LUMINOS Lotus Max and Luminos dRF Max systems with software version VF11 with bucky wall stand for mobile detectors and without ceiling stand .When switching quickly between organ programs (OGPs) the collimation may be incorrect.

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Tags
FDA recall, medical device, class 2, Radiology, Radiation Control for Health and Safety Act, Open, Classified
Related exam domains
CISSP 3: Security Architecture and Engineering; CISSP 8: Software Development Security; CISM 3: Information Security Program
Source record id
Z-0999-2026
First seen by InfoSec Signals
9/23/2026

Exam domain labels come from a keyword heuristic and are study hints, not an official mapping. The summary is the publisher's own text, shortened; the linked record is authoritative.