Olympus recalls EVIS EXERA III bronchovideoscopes (model BF-1TH190) for additional safety instructions when used with laser and plasma equipment. This update ensures safe operation with high-frequency therapy devices.
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 bronchovideoscopes (model BF-:1TH190) because updated safety instructions are needed when using them with laser, argon plasma coagulation, or high-frequency therapy equipment. This recall ensures safe medical procedures by clarifying how these devices interact with specific medical tools.
The bronchovideoscope can interact with laser, argon plasma coagulation, and high-frequency therapy equipment if not used according to updated safety instructions. This interaction could lead to unintended tissue damage or complications during medical procedures.
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.
Check for the model number BF-1TH190 on the device. The recall includes all units sold by Olympus Corporation of the Americas with this model number.
Check for additional safety instructions from Olympus to ensure safe use with laser, argon plasma coagulation, or high-frequency therapy equipment.
Olympus is recalling the EVIS EXERA III bronchovideoscope (model BF-1TH190) for additional safety instructions when used with laser, argon plasma coagulation, or high-frequency therapy equipment.
The recalled product is the EVIS EXERA III bronchovideoscope with model number BF-1TH190. All units sold by Olympus Corporation of the Americas with this model number are affected.
No, the recall does not require stopping use. Healthcare professionals should review the updated safety instructions for safe operation with specific medical equipment.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0049-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0049-2026 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.
