Olymp: EVIS EXERA b Bronchovideoscope model BF-XT190 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 b Bronchovideoscope model BF-XT190 because it can cause endobronchial combustion if used with high-frequency cauterization while oxygen is supplied. This hazard could lead to serious injury during medical procedures.
The device can cause endobronchial combustion when high-frequency cauterization is performed while oxygen is supplied. This occurs if the electrode section of the electrosurgical accessory is too close to the endoscope's tip, potentially causing burns or fire in the airway.
Medical professionals using the EVIS EXERA b Bronchovideoscope model BF-XT190 are most at risk. Patients undergoing procedures with this device may also be affected.
Check for the model number BF-XT190 on the device. The product was sold with a unique identifier (UDI-DI: 4953170402470).
Look for the model number BF-XT190 on the device label.
Yes, there is a risk of endobronchial combustion if high-frequency cauterization is performed while supplying oxygen, which could cause serious injury.
The recall does not specify a remedy, so contact Olympus Corporation of the Americas for further instructions.
Check for the model number BF-XT190 on the device and the unique identifier UDI-DI: 4953170402470.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0193-2024 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0193-2024 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.
