Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Single Use Rotatable Clip Fixing Device Model HX 201LR 135 - Rotatable Recalled by Olympus Corporation of the Americas Due to There have been complaints that the clip did...
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
Single Use Rotatable Clip Fixing Device Model HX 201LR 135 - Rotatable, 165cm long, 2.8 scope channel, standard clip Model HX 201UR 135 - Rotatable, 230 cm long, 2.8 scope channel, standard clip Model HX 201UR 135L - Rotatable, 230 cm long, 2.8 mm scope channel, Long clip
Quantity: 65.9 boxes (373 pieces)
Why Was This Recalled?
There have been complaints that the clip did not come out of the tube sheath during the procedure.
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