Olymp: Olympus recalls EVIS EXERA III Bronchovideoscope (BF-P190) for additional safety updates when used with laser, argon plasma coagulation, and 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 III Bronchovideoscope (model BF-P190) because updated instructions are needed for safe use with certain medical equipment like lasers and plasma coagulation devices. This recall does not involve a physical defect but requires clearer guidance to prevent potential risks during procedures.
The device requires updated instructions for safe use with specific medical equipment. Without these clarifications, there could be risks during procedures involving lasers, plasma coagulation, or high-frequency therapy.
Healthcare professionals using the EVIS EXERA III Bronchovideoscope with laser, argon plasma coagulation, or high-frequency therapy equipment are most at risk. Patients undergoing procedures with this device may also be affected.
The EVIS EXERA III Bronchovideoscope (model BF-P190) is affected. All units sold by Olympus Corporation of the Americas are included in this recall.
Check for additional instructions from Olympus to ensure safe use with laser, argon plasma coagulation, and high-frequency therapy equipment.
No, the recall is for updated instructions to ensure safe use with specific medical equipment, not a physical defect.
No, but you should review the updated instructions for safe use with laser, argon plasma coagulation, and high-frequency therapy equipment.
All EVIS EXERA III Bronchovideoscope (model BF-P190) units sold by Olympus Corporation of the Americas are affected.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0057-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0057-2026 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.
