Olympus recalls EVIS EXERA II Bronchovideoscopes (model BF-P180) for additional safety updates when used with laser and plasma equipment. All units are affected.
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 all EVIS EXERA II Bronchovideoscopes (model BF-P180) because updated safety instructions are needed when using them with laser, argon plasma, or high-frequency therapy equipment. This recall is important because improper use could lead to injury if the equipment isn't used correctly.
The bronchovideoscope can cause injury if used with certain medical equipment without proper safety updates. The hazard is related to incorrect use during procedures involving laser, argon plasma coagulation, or high-frequency therapy.
Healthcare professionals who use the EVIS EXERA II Bronchovideoscope with laser, argon plasma, or high-frequency therapy equipment are most at risk. All units of this model are affected.
Check for the model number BF-P180 on the device. All units are affected, including those with the UDI 4953170339288 and all serial numbers.
Check for additional instructions from Olympus to ensure safe use with laser, argon plasma, or high-frequency therapy equipment.
Yes, all units with model number BF-P180 are affected.
No, but you should review the updated safety instructions before using it with laser, argon plasma, or high-frequency therapy equipment.
Review the latest safety updates from Olympus to ensure safe use with compatible equipment.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0056-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0056-2026 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.
