Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
EVIS EXERA III Gastrointestinal Videoscope Recalled by Olympus Corporation of the Americas Due to Sterilization failures when devices are sterilized per the...
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
EVIS EXERA III Gastrointestinal Videoscope
Quantity: 1687 units
Why Was This Recalled?
Sterilization failures when devices are sterilized per the Reprocessing Manual due to lack of drying time for the endoscope channel.
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