Olympus Bronchofiberscope BF-XP60 Recall: Risk of Loose Instrument Channel Port

Take action

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 Bronchofiberscope BF-XP60 models because attaching non-Olympus accessories might cause the instrument channel port to loosen. This could lead to safety issues during use.

Why it’s dangerous

The instrument channel port may loosen when non-Olympus accessories are attached, potentially causing safety risks during medical procedures. This could happen if the force applied exceeds what the port was designed to handle.

Who’s affected

Medical professionals who use the Bronchofiberscope BF-XP60 are most at risk. All units produced are affected.

How to tell if you have this one

Check for the Bronchofiberscope BF-XP60 model with any lot code. All units are affected by this recall.

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 prevent loosening.

✎ GovInfoNow

Questions people ask

Is this recall affecting all Bronchofiberscope BF-XP60 models?

Yes, all Bronchofiberscope BF-XP60 models are affected by this recall.

What should I do if I have non-Olympus accessories attached?

Ensure all accessories attached to the instrument channel port are Olympus-branded to prevent loosening.

Is there a fix for this issue?

The recall does not specify a fix; users must ensure only Olympus accessories are used.

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-3307-2018 — Olympus Olympus

Hello,

I own a Olympus that is covered by recall Z-3307-2018 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.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

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-3307-2018 (August 8, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3307-2018 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-XP60

Use caution until it’s fixed