Olympus Corporation of the Americas is recalling 67,924 Bronchovideoscope devices across multiple model series, including the BF-1T150, BF-Q180, and EVIS EXERA III lines. The recall was initiated because of a serious risk that the devices can cause internal fires (endobronchial combustion) during medical procedures if high-frequency cauterization is performed while oxygen is being supplied. Consumers and healthcare facilities should immediately review the affected model numbers to ensure safety protocols are updated.
A fire can occur inside the patient's airway if the electrode section of a surgical accessory is too close to the end of the endoscope or if oxygen is being delivered during cauterization. This poses a critical risk of thermal injury to the patient and the healthcare provider.
Risk mitigation through updated safety protocols and manufacturer notification.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.