Olympus recalls EVIS EXERA Bronchovideoscope Olympus BF Type XT160 due to potential safety risks when used with laser and other medical equipment. Affected units require updated instructions for safe use.
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 Bronchovideoscope Olympus BF Type XT:160 models because updated instructions are needed for safe use with certain medical equipment. This recall does not involve immediate danger but ensures proper safety practices when used with laser, argon plasma, or high-frequency therapy devices.
The device requires updated instructions for safe use with laser, argon plasma coagulation, and high-frequency therapy equipment. Without these updates, there could be risks during medical procedures, though the hazard is not severe under normal use.
Healthcare professionals using the Olympus EVIS EXERA Bronchovideoscope Olympus BF Type XT160 for medical procedures are most at risk. Patients receiving care with this device may also be affected if the equipment is used improperly.
Check for the model number BF-XT160 on the device. All units produced by Olympus Corporation of the Americas are affected, including those with the UDI 4953170340147 and all serial numbers.
Check for new instructions from Olympus to ensure safe use with laser and other medical equipment.
No immediate danger is reported. The recall requires updated instructions for safe use with specific medical equipment, but the device itself is not hazardous under normal conditions.
All units with model number BF-XT160 produced by Olympus Corporation of the Americas are affected, including those with UDI 4953170340147 and all serial numbers.
No. The recall requires updated instructions for safe use, not 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-0065-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0065-2026 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.
