Olympus Bronchovideoscope BF-MP6: Non-Olympus Accessories May Cause Port Loosening

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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-MP60 models because attaching non-Olympus accessories can cause the instrument channel port to loosen. This could lead to injury if the port becomes loose during use.

Why it’s dangerous

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

Who’s affected

Healthcare professionals using the Bronchovideoscope BF-MP60 are most at risk. Patients and staff could be affected if the port loosens during procedures.

How to tell if you have this one

Check for the Bronchovideoscope BF-MP60 model with any lot code. The product was 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
Remove any non-Olympus accessories attached to the instrument channel port.
Verify Lot Code
Confirm the lot code on the product to determine if it is affected.

✎ GovInfoNow

Questions people ask

Is this product safe to use with Olympus accessories?

The recall only affects non-Olympus accessories. Olympus accessories should be safe.

What should I do if I have the Bronchovideoscope BF-MP60?

Check for non-Olympus accessories and verify the lot code to see if it is affected.

How can I get a replacement if my product is recalled?

The recall record does not mention a replacement or remedy.

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-3295-2018 — Olympus Olympus

Hello,

I own a Olympus that is covered by recall Z-3295-2018 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-3295-2018 (August 8, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3295-2018 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-MP60

Use caution until it’s fixed