Official recall record
Olympus Bronchovideoscopes
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2025-09-15
- Country of alert
- Canada
- Alert level
- Type I
- Alert type
- recall
What the authority reported
Olympus has determined that additional IFU updates are necessary to provide further clarification on safe and effective use of the bronchoscopes when used in conjunction with laser, argon plasma coagulation, and highfrequency therapy equipment. Users should obtain the updated IFU through Olympus Canada Technical Assistance Center (TAC).
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.