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VISERA™ Imaging System — recall 81587

Health Canada — Medical Devices · Canada · 2026-02-10 · Type II

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Agency: Health Canada — Medical Devices
Recall identifier: 81587
Date of alert: 2026-02-10
Country / jurisdiction: Canada
Risk level: Type II
Risk type: recall
Product category: General hospital and personal use - Gastroenterology and urology
Product type: Medical devices

Reported risk: Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of MAJ-210 and MAJ-1218. Olympus is highlighting the importance of strictly adhering to the IFU. Olympus will share an updated customer notification by mid-2026.

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/viseratm-imaging-system

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VISERA™ Imaging System — recall 81587

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