Health product recall

OES Pro Urology Resection Sheaths

Last updated

Summary

Product
OES Pro Urology Resection Sheaths
Issue
Medical devices - Device compatibility
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

OES Pro Urology Resection Sheaths

More than 10 numbers, contact manufacturer.

WA22810A

Issue

Olympus has received six complaints about a damaged tip during use of a laser probe. Olympus has not received any reported injuries related to this matter. As a result of this complaint investigation, Olympus is removing the statement of compatibility with a greenlight laser for BPH therapy from the instructions for use (IFU) until Olympus can conduct additional testing.

Recall Start Date: October 11, 2024

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Gastroenterology and urology
Companies

Olympus Winter & Ibe Gmbh

Kuehnstrasse 61, Hamburg, Hamburg, Germany, 22045

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-76413

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