Olympus Bronchovideoscope BF-3C40 Recall: Risk of Loose Instrument Channel Port

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Contact the company & request your remedy

Recalling firmOlympus Corporation of the Americas3500 Corporate Pkwy, PO Box 610 · Center Valley, PA 18034-0610

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Olympus is recalling all Bronchovideoscope BF-3C40 models due to a risk that non-Olympus accessories could cause the instrument channel port to loosen. This could potentially lead to safety issues during medical procedures.

Why it’s dangerous

The attachment of non-Olympus accessories to the instrument channel port may apply more force than expected, causing the port to loosen. This could lead to safety issues during medical procedures if the port becomes loose.

Who’s affected

Medical professionals using the Bronchovideoscope BF-3C40 are likely affected. Those who attach non-Olympus accessories to the device face the highest risk.

How to tell if you have this one

Check for the Bronchovideoscope BF-3C40 model with any lot code. The recall applies to all units produced.

Brand
Olympus
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check for Non-Olympus Accessories
Ensure no non-Olympus accessories are attached to the instrument channel port.

✎ GovInfoNow

Questions people ask

Is there a fix for this issue?

The recall notice does not state any remedy or fix for this issue.

Which models are affected?

All Bronchovideoscope BF-3C40 models with any lot code are affected.

How can I tell if my device is recalled?

Check for the Bronchovideoscope BF-3C40 model with any lot code. The recall applies to all units.

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-3291-2018 — Olympus Olympus

Hello,

I own a Olympus that is covered by recall Z-3291-2018 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-3291-2018 (August 8, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3291-2018 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 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 Bronchovideoscope BF-3C40

Recall notice