Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Endocuff Vision: models ARV 110 Recalled by Boddingtons Plastics Ltd Due to Updated Instructions For Use- to contraindications and potential...
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 Boddingtons Plastics Ltd directly.
Affected Products
Endocuff Vision: models ARV 110, 120, 130, 140 Intended Use: ENDOCUFF VISION is a device attached to the distal end of a colonoscope, designed to maintain and maximize the viewable mucosa during endocosopic therapy by manipulating colonic folds
Quantity: 13202 Units US
Why Was This Recalled?
Updated Instructions For Use- to contraindications and potential complications/adverse events of the colonoscopy procedure (without using Endocuff Vision Device)
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Boddingtons Plastics Ltd
Boddingtons Plastics Ltd has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report