Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ENF-GP2 Rhino-Laryngo Fiberscope - Product Usage: is indicated for use Recalled by Olympus Corporation of the Americas Due to Products repaired with the incorrect service manual may...
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
ENF-GP2 Rhino-Laryngo Fiberscope - Product Usage: is indicated for use within the nasal and nasopharyngeal lumen.
Quantity: 19
Why Was This Recalled?
Products repaired with the incorrect service manual may be missing an O ring and are subject to rework with the corrected service manual.
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