Olympus recalls its BF MP60 bronchoscopes for updated safety instructions when used with laser, plasma coagulation, or high-frequency therapy equipment to prevent risks during 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.
Olymp: Olympus is recalling its BF MP60 bronchoscopes because they require updated safety instructions when used with certain medical equipment like lasers or plasma coagulation devices. This recall is important because improper use could lead to risks during medical procedures.
The bronchoscope may pose risks if not used with updated safety instructions when paired with laser, argon plasma coagulation, or high-frequency therapy equipment. This could lead to complications during medical procedures if the equipment is not properly managed.
Healthcare professionals using Olympus BF MP60 bronchoscopes for procedures involving lasers, plasma coagulation, or high-frequency therapy equipment are most at risk. Patients undergoing these procedures may also be affected if the equipment is used incorrectly.
Check for the Olympus BF MP60 model with serial numbers listed in the recall notice. The product is sold under the brand name Olympus and was distributed through medical channels.
Check for additional instructions from Olympus to ensure safe use with laser, plasma coagulation, or high-frequency therapy equipment.
This recall applies to healthcare professionals using the bronchoscope in procedures with specific medical equipment. Patients are not directly affected by this recall.
Olympus has not provided a specific remedy for this recall. You should review the updated safety instructions if you use the device with laser, plasma coagulation, or high-frequency therapy equipment.
The recall states that additional safety updates are needed when using the bronchoscope with specific medical equipment. Normal use without these equipment may not pose a risk.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0054-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0054-2026 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.
