Olympus recalls specific bronchovideoscope models due to risk of endoscope becoming lodged in endotracheal tube connectors, potentially causing breathing issues.
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Olympus is recalling three bronchovideoscope models because they may become lodged in endotracheal tube connectors, which could block breathing. This is a serious hazard for medical staff using the devices during procedures.
The endoscope's diameter is too large for the endotracheal tube connector, causing it to become lodged. This can block the airway, leading to breathing difficulties or other complications during medical procedures.
Healthcare professionals using these bronchovideoscopes during medical procedures are most at risk. Patients receiving care with these devices could also be affected.
Check for the model numbers BF-MP160F, BF-XP160F, or BF-XP60 on the device. These bronchovideoscopes were sold with specific serial numbers and UDI-DI codes listed in the recall notice.
Immediately stop using the recalled bronchovideoscopes as they may become lodged in endotracheal tube connectors, blocking the airway.
The recalled models are Olympus Bronchovideoscope, Models BF-MP160F, BF-XP160F, and BF-XP60.
Check for the model numbers BF-MP160F, BF-XP160F, or BF-XP60 on the device. These models were sold with specific serial numbers and UDI-DI codes listed in the recall notice.
Immediately stop using the device as it may become lodged in endotracheal tube connectors, blocking the airway. Contact Olympus for further instructions.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-2491-2023 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-2491-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
