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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.

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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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