CanadaOES Pro Urology Resection Sheaths (cystoscope outer sheath, 22.5 Fr; model/catalogue WA22810A, all lots) from Olympus Winter & Ibe GmbH are affected. Olympus has initiated a voluntary recall and asks users to immediately cease use of any 22.5 Fr cystoscope outer sheath and contact customer service to obtain a return material authorization, and to contact the manufacturer for additional information.
What's being recalled
Companies: Olympus Winter & Ibe Gmbh, Kuehnstrasse 61, Hamburg, Hamburg, Germany, 22045.
How to identify it
Affected products: OES Pro Urology Resection Sheaths; Lot or serial number: All lots.; Model or catalogue number: WA22810A
The hazard
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.
What to do
Contact the manufacturer if you require additional information.
The official notice
This page is a summary of the notice published by Health Canada, collected from Health Canada, CFIA and Transport Canada. Check the original before you act on it.
Read the official notice (opens in a new tab)