Olympus Bronchovideoscope Models BF-3C4: Risk of Getting Stuck in Airway

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Recalling firmOlympus Corporation of the Americas3500 Corporate Pkwy, N/A · Center Valley, PA 18034-8229

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Olympus is recalling two bronchovideoscope models (BF-3C40 and BF-N20) because they might get stuck in endotracheal tubes during medical procedures. This could block the airway and cause serious breathing problems for patients.

Why it’s dangerous

The bronchovideoscope's diameter is too large for the endotracheal tube connector, which can cause it to become lodged during medical procedures. This may block the airway and prevent proper breathing for patients.

Who’s affected

Healthcare professionals using these scopes during medical procedures are most at risk. Patients receiving care with these scopes could also be affected if the scope becomes lodged.

How to tell if you have this one

Check for the model numbers BF-3C40 or BF-N20 on the device. The product was sold with specific serial numbers and UDI-DI codes listed in the recall notice.

Brand
Olympus
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Model
Look for the model numbers BF-3C40 or BF-N20 on the bronchovideoscope.

✎ GovInfoNow

Questions people ask

Why is this recall happening?

The bronchovideoscope models might become lodged in the endotracheal tube connector due to their diameter being too large, which could block the airway.

What should healthcare providers do?

Healthcare providers should check if they have the recalled models and contact Olympus for guidance on next steps.

Is there a fix for this issue?

The recall record does not mention a specific fix or remedy for this issue.

Take action

Contact Olympus

We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-2502-2023 — Olympus Olympus

Hello,

I own a Olympus that is covered by recall Z-2502-2023 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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Where this comes from

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.

Official source: FDA Recall #Z-2502-2023 (July 27, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2502-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Olympus Corporation of the Americas recalls Olympus Bronchovideoscope, Models BF-3C40 & BF-N20.

Use caution until it’s fixed