Olympus Bronchovideoscope BF-MP16: 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

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

Olympus is recalling bronchovideoscopes model BF-MP160F because non-Olympus accessories might loosen the instrument channel port, potentially causing injury during use. This affects all units sold with any lot code.

Why it’s dangerous

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

Who’s affected

Healthcare professionals using the bronchovideoscope are most at risk if they attach non-Olympus accessories. Patients may be affected if the device is used improperly.

How to tell if you have this one

Check for the Olympus Bronchovideoscope BF-MP160F model with any lot code. The product was sold under the brand name Olympus.

Brand
Olympus
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check for Non-Olympus Accessories
Look for non-Olympus accessories attached to the instrument channel port.
Stop Using if Loose Port
If the instrument channel port feels loose, stop using the device immediately.

✎ GovInfoNow

Questions people ask

Is this recall affecting patients directly?

The recall affects healthcare professionals using the device, but patients may be impacted if the device is used improperly.

How can I tell if my bronchovideoscope is affected?

Check for the Olympus Bronchovideoscope BF-MP160F model with any lot code.

What should I do if the port is loose?

If the instrument channel port feels loose, stop using the device immediately.

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-3294-2018 — Olympus Olympus

Hello,

I own a Olympus that is covered by recall Z-3294-2018 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-3294-2018 (August 8, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3294-2018 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 Bronchovideoscope BF-MP160F

Use caution until it’s fixed