Official recall record
OES Pro Urology Resection Sheaths (ref 76413)
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-10-30
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
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
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
ProductGuru Recalls republishes official safety information with attribution. We are not
the issuing authority and this page is not advice. If this product is a medical device or
medication, speak to a doctor or pharmacist. Found an error?
Report it — corrections are published.