Olympus recalls EVIS EXERA III Bronchovideoscopes (BF-Q190) for safety updates when used with laser and plasma equipment. No immediate action needed but follow 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 III Bronchovideoscopes (model BF-Q190) because additional safety instructions are needed when using them with laser, argon plasma, or high-frequency therapy equipment. This recall does not involve a physical defect but requires updated safety procedures to prevent potential risks during medical procedures.
The device requires updated safety instructions when used with laser, argon plasma coagulation, or high-frequency therapy equipment. Without these updates, there could be risks during medical procedures, though the hazard is not described as causing serious injury in normal use.
Healthcare professionals using the EVIS EXERA III Bronchovideoscope (model BF-Q190) with laser or plasma equipment are most at risk. Patients undergoing procedures with this device may also be affected if safety protocols are not followed.
Check for the model number BF-Q190 on the device. The recall includes all units with serial numbers listed in the UDI (4953170434792, 4953170335198).
Check the device for updated safety instructions when used with laser, argon plasma, or high-frequency therapy equipment.
No, the recall does not require immediate discontinuation. Additional safety instructions are needed for safe use with certain equipment.
Review the updated safety instructions for use with laser, argon plasma, or high-frequency therapy equipment as provided by Olympus.
The recall describes a need for updated safety instructions but does not specify a risk of serious injury in normal use.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0063-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0063-2026 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.
