Olympus Bronchovideoscope BF-XT160 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 its Bronchovideoscope BF-XT16:0 models because attaching non-Olympus accessories might cause the instrument channel port to loosen. This could lead to safety issues during medical procedures.

Why it’s dangerous

When non-Olympus accessories are attached to the instrument channel port, the device may experience more force than expected. This can cause the port to loosen, potentially leading to safety risks during medical procedures.

Who’s affected

Healthcare professionals using the Bronchovideoscope BF-XT160 for medical procedures are most at risk. Patients undergoing procedures with this device may also be affected.

How to tell if you have this one

Check for the Bronchovideoscope BF-XT160 model with any lot code. The product is 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 Instrument Channel Port
Inspect the instrument channel port for signs of looseness or damage.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

The attachment of non-Olympus accessories to the instrument channel port may cause more force than expected, leading to loosening of the port.

What models are affected?

All Bronchovideoscope BF-XT160 models with any lot code.

Is there a fix for this issue?

The recall does not specify a fix; users should check the port for looseness.

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-3308-2018 — Olympus Olympus

Hello,

I own a Olympus that is covered by recall Z-3308-2018 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-3308-2018 (August 8, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3308-2018 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-XT160

Use caution until it’s fixed