Olympus recalls bronchovideoscopes with model BF-1T150 for safety updates when used with laser, argon plasma, or high-frequency therapy equipment. No immediate action needed but updates are critical for safe medical 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.
Olympus is recalling bronchovideoscopes with model number BF- 1T150 due to the need for additional safety instructions when used with certain medical equipment like lasers. This recall is important because improper use could lead to risks during procedures.
The device requires specific safety updates when used with certain medical equipment. Without these updates, there is a risk of complications during procedures, but the hazard is not immediately dangerous in normal use.
Healthcare professionals using the bronchovideoscope with laser, argon plasma coagulation, or high-frequency therapy equipment. Patients undergoing procedures with this device may be at risk if instructions are not followed.
Check for model number BF-1T150 on the device. The recall includes all units sold by Olympus Corporation of the Americas with this model.
Olympus has provided additional instructions for safe use with laser, argon plasma coagulation, and high-frequency therapy equipment.
No, but you must follow the updated safety instructions for use with specific medical equipment.
The recall addresses safety updates for procedures, not an immediate risk to patients if used correctly.
Look for model number BF-1T150 on the device; all units sold by Olympus Corporation of the Americas are included.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0045-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0045-2026 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.
