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FDA device recallVulnerabilitiesPublished March 27, 2026
Reflexion Medical, Inc.: Fludeoxyglucose F18-Guided Radiation Therapy System
Due to a radiotherapy medical system software defect, when performing angular roll corrections followed by a repeat localization, the roll corrections applied in the initial localization scan are not carried through to treatment delivery leading to the treatment plan dose being delivered to the incorrect location, potentially a displacement of 5mm or higher, with a 10% to 20% underdose.
Open the source record- Tags
- FDA recall, medical device, class 2, Radiology, Software change control, 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-1656-2026
- First seen by InfoSec Signals
- 9/23/2026
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