Product Wiki · Recalls · Health Canada — Medical Devices

Olympus Resection and Inner Sheaths — recall 81489

Health Canada — Medical Devices · Canada · 2026-01-16 · Type II

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →

Agency: Health Canada — Medical Devices
Recall identifier: 81489
Date of alert: 2026-01-16
Country / jurisdiction: Canada
Risk level: Type II
Risk type: recall
Product category: Gastroenterology and urology
Product type: Medical devices

Reported risk: Olympus has identified complaints related to the ceramic tip of the resection/inner sheath breaking. Olympus is highlighting the importance of strictly adhering to the 'inspection and testing' and 'caution' sections in the IFU for the resection/inner sheath, and the 'inspection before each use' section in the resectoscope system manual.

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/olympus-resection-and-inner-sh

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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.

Olympus Resection and Inner Sheaths — recall 81489

Related