Olympus recalls BF-H1100 bronchovideoscopes for safety updates when used with laser, argon plasma, or high-frequency therapy equipment. No immediate action needed but updates required 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 BF-H1100 bronchovideoscopes because additional safety instructions are needed when using them with laser, argon plasma coagulation, or high-frequency therapy equipment. This recall ensures safe medical procedures but does not pose an immediate risk to users.
The bronchovideoscope may not function safely when used with certain medical equipment like lasers or argon plasma coagulation devices without updated instructions. This could lead to improper use or complications during procedures if the device is not properly maintained.
Healthcare professionals using the Olympus BF-H1100 bronchovideoscopes with laser, argon plasma, or high-frequency therapy equipment are most at risk. Patients using these devices under medical supervision are not directly affected.
Check for the model number BF-H1100 on the device. All units are affected, including those with serial numbers and the UDI 4953170424229.
Olympus will provide additional instructions for safe use with laser, argon plasma, and high-frequency therapy equipment.
No immediate danger is reported; the recall requires updated safety instructions for specific medical equipment use.
No, but you must follow updated safety instructions when using the device with laser, argon plasma, or high-frequency therapy equipment.
All Olympus BF-H1100 bronchovideoscopes are affected, as indicated by the model number and UDI 4953170424229.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0052-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0052-2026 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.
