Olympus recalls EVIS EXERA II bronchovideoscopes (model BF-1TQ180) for updated safety instructions when used with laser, plasma, or high-frequency therapy equipment.
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 bronchovideoscopes (model BF-1TQ18:1TQ180) because additional safety instructions are needed when using them with laser, argon plasma coagulation, or high-frequency therapy equipment. This recall addresses potential risks from improper use with these devices.
The bronchovideoscope can pose risks if not used with proper safety protocols when combined with laser, argon plasma coagulation, or high-frequency therapy equipment. This may lead to complications if the equipment is not correctly configured or maintained.
Healthcare professionals who use the EVIS EXERA II bronchovideoscopes with laser, argon plasma coagulation, or high-frequency therapy equipment are most at risk. Patients using these devices under medical supervision are also affected.
Check for the model number BF-1TQ180 on the device or its packaging. The recall includes all units sold by Olympus Corporation of the Americas.
Check the device for updated safety instructions from Olympus Corporation of the Americas regarding use with laser, argon plasma coagulation, and high-frequency therapy equipment.
The recall is for updated safety instructions, not a safety hazard. The risk is low as it addresses proper use with specific medical equipment.
No, you do not need to stop using it. The recall requires updated safety instructions for proper use with laser, argon plasma coagulation, or high-frequency therapy equipment.
Review the updated safety instructions from Olympus Corporation of the Americas to ensure safe use with laser, argon plasma coagulation, or high-frequency therapy equipment.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0051-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0051-2026 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.
