Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Olympus EVIS EXERA BRONCHOVIDEOSCOPE BF TYPE Recalled by Olympus Corporation of the Americas Due to There have been complaints of endobronchial combustion during...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Olympus Corporation of the Americas directly.
Affected Products
Olympus EVIS EXERA BRONCHOVIDEOSCOPE BF TYPE, Model Number BF-XT160
Quantity: 284 units
Why Was This Recalled?
There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Olympus Corporation of the Americas
Olympus Corporation of the Americas has 378 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report