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Health Canada Medical devices

EXENT® Analyser

Issued April 16, 2026
Issue
Product EXENT® Analyser Issue Medical devices - Performance What to do Contact the manufacturer if you require additional information. Audience Healthcare
Hazard description
FSCA initiated due to a software issue affecting the EXENT® Analyser (IE800), whereby QC may not be performed but is indicated as complete under specific conditions, potentially allowing unverified results to be reported. Users are advised to review QC results and audit logs to confirm that QC has been performed.
Reference
ID
RA-81992