Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
EVIS EXERA II Duodenovideoscope OLYMPUS TJF TypeQ180V. This instrument has Recalled by Olympus America Inc. Due to New and validated reprocessing procedures have been issued...
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 America Inc. directly.
Affected Products
EVIS EXERA II Duodenovideoscope OLYMPUS TJF TypeQ180V. This instrument has been designed to be used with an Olympus video system center, light source, documentation equipment, monitors, EndoTherapy accessories (such as a biopsy forceps), and other ancillary equipment for endoscopy and endoscopic surgery within the duodenum.
Quantity: 6109
Why Was This Recalled?
New and validated reprocessing procedures have been issued for the Olympus TJF-Q180V duodenoscope ("TJF-Q180V"), consisting of revised manual cleaning and high level disinfection procedures.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Olympus America Inc.
Olympus America Inc. has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report