Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BF-XP60 OES Bronchofiberscope Recalled by Olympus Corporation of the Americas Due to The firm is issuing validated, new reprocessing instructions...
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
BF-XP60 OES Bronchofiberscope, Model No. BF-XP60
Quantity: 180
Why Was This Recalled?
The firm is issuing validated, new reprocessing instructions according to the FDA 2015 guidance, "Reprocessing Medical Devices in Health Care Settings: Validation Methods and Labeling."
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