Product Wiki · Recalls · Health Canada — Medical Devices

Olympus Medical Single Use Electrosurgical Snare SD-400 — recall 78388

Health Canada — Medical Devices · Canada · 2025-10-30 · 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 on this page. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
78388
Date of alert
2025-10-30
Country / jurisdiction
Canada
Authority classification
Type II
Notice type
recall
Product category
General and plastic surgery
Product type
Medical devices
Reported risk: Olympus's investigation determined that small holes may occur during packaging of SD-400 device pouches into the shelf carton and/or during transportation of the shelf carton. Users should cease usage of the affected lots immediately due to the potential sterility breach.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/olympus-medical-single-use-ele

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.