Olympus recalls EVIS EXERA II Bronchovideoscope (Model BF-Q180) for additional safety updates when used with laser, argon plasma, or high-frequency therapy equipment. No immediate action required but updates are needed for safe use.
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
Olympus is recalling its EVIS EXERA II Bronchovideoscope (model BF-Q180) because updated safety instructions are needed when using it with certain medical equipment like lasers or argon plasma. This recall does not involve immediate danger but ensures safe medical procedures.
The device requires updated safety instructions when used with specific medical equipment such as lasers, argon plasma coagulation, or high-frequency therapy. Without these updates, there could be risks during medical procedures, though the hazard is not immediately dangerous.
Healthcare professionals using the EVIS EXERA II Bronchovideoscope with laser, argon plasma coagulation, or high-frequency therapy equipment. Patients undergoing procedures with this device may be at risk if safety updates are not followed.
Check for the model number BF-Q180 on the device or its packaging. The recall includes all units sold by Olympus Corporation of the Americas with this model.
Check for additional instructions from Olympus to ensure safe use with laser, argon plasma, or high-frequency therapy equipment.
No immediate danger is reported. The recall requires updated safety instructions for specific medical equipment use, but the device itself is not hazardous.
No. The recall does not require stopping use but requires updated safety instructions for specific medical equipment.
The recalled model is EVIS EXERA II Bronchovideoscope with model number BF-Q180, sold by Olympus Corporation of the Americas.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0061-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0061-2026 from Olympus. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
