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EVIS EXERA III Duodenovideoscope — recall 81566

Health Canada — Medical Devices · Canada · 2026-02-03 · Type I

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Agency: Health Canada — Medical Devices
Recall identifier: 81566
Date of alert: 2026-02-03
Country / jurisdiction: Canada
Risk level: Type I
Risk type: recall
Product category: Gastroenterology and urology
Product type: Medical devices

Reported risk: Olympus has updated the reprocessing materials to minimize potential deviations in TJF duodenoscope reprocessing. Olympus is informing users of these changes and is reminding users to closely follow the operation and reprocessing instructions. Users are required to acknowledge reviewing all such materials, which can be accessed through Olympus' education portal.

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/evis-exera-iii-duodenovideosco

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EVIS EXERA III Duodenovideoscope — recall 81566

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