Olympus recalls its Bronchofibercope Olympus BF Type 1T60 for additional safety instructions when used with laser, plasma coagulation, or 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 Bronchofibercope Olympus BF Type 1T60 to provide clearer safety instructions for use with laser, argon plasma coagulation, and high-frequency therapy equipment. This update helps prevent potential risks when these devices are used together.
The bronchoscope can pose risks when used with certain medical equipment like lasers, argon plasma coagulation, or high-frequency therapy devices. The hazard comes from potential interactions that could lead to complications during procedures.
Healthcare professionals using the Olympus Bronchofibercope Olympus BF Type 1T60 with laser, plasma coagulation, or high-frequency therapy equipment. Those most at risk are medical staff performing procedures requiring these tools.
Check for the model number BF-1T60 on the device. The recall includes all units with this model and serial numbers.
Read the updated instructions for safe use with laser, plasma coagulation, and high-frequency therapy equipment.
Yes, the Olympus Bronchofibercope Olympus BF Type 1T60 model is recalled.
No, the recall requires updated safety instructions, not immediate discontinuation.
The recall does not require discarding or returning the device; it provides updated safety instructions.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0047-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0047-2026 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.
