Olympus Bronchovideoscope Model BF-MP190F Recall: Risk of Getting Stuck in Tube

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Contact the company & request your remedy

Recalling firmOlympus Corporation of the Americas3500 Corporate Pkwy, N/A · Center Valley, PA 18034-8229

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

Olympus is recalling its Bronchovideoscope model BF-MP1:90F because it can get stuck in endotracheal tube connectors. This could cause breathing problems for patients during medical procedures.

Why it’s dangerous

The endoscope's diameter is too large for the endotracheal tube connector, which can cause it to become lodged. This may block the airway and lead to breathing difficulties during medical procedures.

Who’s affected

Healthcare professionals using the Olympus Bronchovideoscope model BF-MP190F for medical procedures are most at risk. Patients receiving care with this model could be affected.

How to tell if you have this one

Check for the model number BF-MP190F on the device. Affected units have specific serial numbers and UDI-DI code 04953170395581.

Brand
Olympus
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Model
Look for the model number BF-MP190F on the Olympus Bronchovideoscope.
Contact Manufacturer
Reach out to Olympus Corporation of the Americas for further assistance with the recall.

✎ GovInfoNow

Questions people ask

Is this product dangerous for home use?

This product is for medical use only and is not intended for home use.

How can I tell if my device is affected?

Check for the model number BF-MP190F and the UDI-DI code 04953170395581 on the device.

What should I do if I have this device?

Contact Olympus Corporation of the Americas for guidance on next steps.

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-2497-2023 — Olympus Olympus

Hello,

I own a Olympus that is covered by recall Z-2497-2023 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-2497-2023 (July 27, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2497-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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 Olympus Bronchovideoscope, Models BF-MP190F.

Use caution until it’s fixed