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FDA device recallVulnerabilitiesPublished October 21, 2025

Beckman Coulter, Inc.: Radioimmunoassay, Thyroid-Stimulating Hormone

Beckman Coulter has confirmed a software anomaly on DxI 9000 Access Immunoassay Analyzer and the DxC 500i Clinical Analyzer that may prevent correct application of user-specified manual dilution factors when ordering additional tests for samples already "In Progress" using the same "Sample ID number". This can lead to false low or high patient results and potential delays in reporting, risking erroneous diagnoses if undetected.

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Tags
FDA recall, medical device, class 2, Clinical Chemistry, Software design, Open, Classified
Related exam domains
CISSP 3: Security Architecture and Engineering; CISSP 8: Software Development Security
Source record id
Z-0216-2026
First seen by InfoSec Signals
9/23/2026

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