Olymp: EVIS EXERA III Bronchovideoscope model BF-P190 recalled due to risk of endobronchial combustion during high-frequency cauterization with oxygen.
There is a risk of endobronchial combustion if high-frequency cauterization is performed while supplying oxygen [and/or] the electrode section of the electrosurgical accessory is too close to the distal end of the endoscope.
Olympus is recalling its EVIS EXERA III Bronchovideoscope model BF-P190 because improper use during high-frequency cauterization with oxygen could cause endobronchial combustion. This hazard may lead to serious injury if the electrosurgical electrode is too close to the endoscope tip.
The hazard occurs when high-frequency cauterization is performed while oxygen is supplied, and the electrosurgical electrode is too close to the endoscope tip. This can cause the tissue to ignite and burn, potentially leading to serious injury.
Healthcare professionals using the EVIS EXERA III Bronchovideoscope for bronchoscopy procedures are most at risk. Patients undergoing procedures with this device could also be affected.
Check for the model number BF-P190 on the device. The recall includes units sold with UDI-DI: 4953170342110.
Look for the model number BF-P190 on the device or its packaging.
Yes, if high-frequency cauterization is performed while supplying oxygen and the electrode is too close to the endoscope tip, it can cause endobronchial combustion.
The recall does not specify a remedy, so contact Olympus Corporation of the Americas for further instructions.
Check for the model number BF-P190 and UDI-DI: 4953170342110 on the device or its packaging.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0194-2024 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0194-2024 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.
