Olympus recalls BF Type TE2 bronchoscopes for safety updates when used with laser, plasma coagulation, or high-frequency therapy equipment. Learn if your device is affected and what to do.
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 BF Type TE2 bronchoscopes because additional safety instructions are needed when using them with laser, plasma coagulation, or high-frequency therapy equipment. This recall addresses potential safety risks during medical procedures.
The bronchoscope could pose safety risks if used with certain medical equipment like lasers, plasma coagulation devices, or high-frequency therapy tools without updated safety instructions. This may lead to complications during procedures if not properly managed.
Healthcare professionals who use Olympus BF Type TE:2 bronchoscopes with laser, plasma coagulation, or high-frequency therapy equipment are most at risk. Patients undergoing procedures with these devices may also be affected.
Check for the model number BF-TE2 on the device. The recall includes all units with serial numbers and the unique device identifier 4953170339998.
Check for additional safety updates from Olympus to ensure proper use with laser, plasma coagulation, or high-frequency therapy equipment.
The recall applies to healthcare providers using the bronchoscopes with specific medical equipment. Patients are not directly affected by this recall.
Look for the model number BF-TE2 on the device. The recall includes all units with serial numbers and the unique device identifier 4953170339998.
No, the recall requires updated safety instructions but does not require immediate discontinuation of use.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0064-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0064-2026 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.
