Olympus recalls specific bronchovideoscope models due to risk of the endoscope becoming lodged in the endotracheal tube connector, potentially causing breathing issues during medical procedures.
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Olympus is recalling four bronchovideoscope models because the endoscope's diameter may be too large, causing it to get stuck in the endotracheal tube connector. This could lead to breathing problems during medical procedures if the device is used incorrectly.
The endoscope's diameter is too large for the endotracheal tube connector, which can cause it to become lodged during use. This may block the airway and lead to breathing problems if the device is not properly secured or removed.
Healthcare professionals using the Olympus bronchovideoscopes for medical procedures are most at risk. Patients undergoing procedures with these devices could experience breathing difficulties if the endoscope becomes lodged.
Check for the model numbers BF-1TH190, BF-H190, BF-Q170, or BF-Q190 on the device. The recall includes all serial numbers and uses specific UDI-DI codes listed in the notice.
Identify the model number on the bronchovideoscope to see if it matches BF-1TH190, BF-H190, BF-Q170, or BF-Q190.
Reach out to Olympus Corporation of the Americas for further instructions on the recall process.
The recall is due to complaints that the endoscope model can become lodged in the endotracheal tube connector because its diameter is too large.
Check the model number to see if it's affected, then contact Olympus Corporation of the Americas for instructions.
The recall indicates a risk of the endoscope becoming lodged, which could cause breathing problems during medical procedures, but the remedy does not specify immediate action to stop use.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-2496-2023 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-2496-2023 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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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.
