Olympus recalls EVIS EXERA II bronchovideoscopes (model BF-1T18:180) for safety updates when used with laser, plasma coagulation, or high-frequency therapy equipment. No immediate action needed but updates are critical 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 bronchovideoscopes (model BF-1T180) because additional safety instructions are needed when using them with laser, plasma coagulation, or high-frequency therapy equipment. This recall is to prevent potential risks during medical procedures.
The bronchovideoscope can pose risks if used with certain medical equipment like lasers, plasma coagulation, or high-frequency therapy without proper safety updates. This could lead to complications during procedures if the equipment is not used according to updated safety guidelines.
Healthcare professionals using the EVIS EXERA II bronchovideoscopes with laser, plasma coagulation, or high-frequency therapy equipment. Patients undergoing procedures with these devices may be at risk if the equipment is not used correctly.
Check for the model number BF-1T180 on the device or the label. The recall includes all units with serial numbers and the UDI 4953170339325.
Check for additional instructions from Olympus to ensure safe use with laser, plasma coagulation, or high-frequency therapy equipment.
No, the recall does not require stopping use. Additional safety instructions are needed for proper use with specific medical equipment.
Review the latest safety updates from Olympus to ensure safe use with laser, plasma coagulation, or high-frequency therapy equipment.
The recall indicates potential risks if the device is used without updated safety instructions with certain medical equipment, but no specific injuries have been reported.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0046-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0046-2026 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.
