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FDA device recallVulnerabilitiesPublished August 10, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Interventional Fluoroscopic X-Ray System
Two software related issues affecting Azurion R2.2.10 Systems: 1) Potential image quality degradation that may lead to delay of therapy, procedural complications and/or inappropriate treatment and 2) Potential loss of geometry movements that may lead to delay of therapy and procedural complications
Open the source record- Tags
- FDA recall, medical device, class 2, Radiology, Software design, Open, Classified
- Related exam domains
- CISSP 3: Security Architecture and Engineering; CISSP 8: Software Development Security
- Source record id
- Z-2931-2026
- First seen by InfoSec Signals
- 9/23/2026
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