Olympus recalls EVIS EXERA II bronchovideoscopes for updated safety instructions when used with laser, argon plasma, or high-frequency therapy equipment to prevent risks during procedures.
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.
Olymp: Olympus is recalling its EVIS EXERA II bronchovideoscopes to provide clearer safety instructions when used with laser, argon plasma coagulation, or high-frequency therapy equipment. This update helps prevent potential risks during medical procedures.
The bronchovideoscope can pose risks when used with certain medical equipment like lasers, argon plasma coagulation devices, or high-frequency therapy equipment. The hazard is related to improper use during procedures, which could lead to complications.
Healthcare professionals using the EVIS EXERA II bronchovideoscopes for procedures involving laser, argon plasma, or high-frequency therapy equipment. Patients undergoing these procedures may be at risk if the equipment is not used correctly.
The EVIS EXERA II bronchovideoscope with model number BF-Q180-AC and all serial numbers. This product was sold by Olympus Corporation of the Americas.
Check for updated safety instructions provided by Olympus to ensure proper use with laser, argon plasma, or high-frequency therapy equipment.
The recall is for healthcare professionals using the bronchovideoscope during procedures. Patients are not directly affected by this recall.
No, the recall does not require stopping use. Instead, Olympus is providing updated safety instructions for proper use with specific medical equipment.
Review the updated safety instructions from Olympus to ensure safe use with laser, argon plasma, 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-0062-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0062-2026 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.
