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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.
Open the source record- 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
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