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OES Pro Urology Resection Sheaths — recall 81522

Health Canada — Medical Devices · Canada · 2026-01-23 · Type II

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Agency: Health Canada — Medical Devices
Recall identifier: 81522
Date of alert: 2026-01-23
Country / jurisdiction: Canada
Risk level: Type II
Risk type: recall
Product category: Gastroenterology and urology
Product type: Medical devices

Reported risk: Further to the FY25-022 medical device recall issued in October 2024, Olympus is informing users of a voluntary product recall action for cystoscope outer sheath. Users should immediately cease usage of any cystoscope outer sheath, 22.5 Fr in your inventory and contact customer service to obtain a return material authorization.

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/oes-pro-urology-resection-shea

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

OES Pro Urology Resection Sheaths — recall 81522

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