Olympus Bronchofiberscope BF-XT4: Non-Olympus Attachments May Cause Port Loosening

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

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Olympus is recalling all Bronchofiberscope BF-XT40 models due to a risk that non-Olympus accessories could loosen the instrument channel port, potentially causing injury during medical procedures.

Why it’s dangerous

Non-Olympus accessories attached to the instrument channel port can apply more force than expected, causing the port to loosen. This could lead to injury during medical procedures if the port becomes dislodged.

Who’s affected

Medical professionals using the Bronchofiberscope BF-XT40 are most at risk. Patients undergoing procedures with this device may also be affected if non-Olympus accessories are used.

How to tell if you have this one

Check for the Bronchofiberscope BF-XT40 model with any lot code. The recall applies to all units sold by Olympus Corporation of the Americas.

Brand
Olympus
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check for Non-Olympus Accessories
Ensure all accessories attached to the instrument channel port are Olympus-branded to avoid loosening risks.

✎ GovInfoNow

Questions people ask

Is this recall for all Bronchofiberscope BF-XT40 models?

Yes, Olympus recalls all Bronchofiberscope BF-XT40 models with any lot code.

What could happen if the port loosens?

The port loosening could cause injury during medical procedures if the instrument channel becomes dislodged.

Do I need to stop using the device immediately?

No, but you should check for non-Olympus accessories and ensure they are Olympus-branded to prevent port loosening.

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-3309-2018 — Olympus Olympus

Hello,

I own a Olympus that is covered by recall Z-3309-2018 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-3309-2018 (August 8, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3309-2018 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 Bronchofiberscope BF-XT40

Use caution until it’s fixed