Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Fuse 1C Colonoscope Recalled by EndoChoice, Inc. Due to The bending section of the device may partially...
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 EndoChoice, Inc. directly.
Affected Products
Fuse 1C Colonoscope
Quantity: 253 units
Why Was This Recalled?
The bending section of the device may partially separate from the insertion tube. Potential for tissue trauma.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About EndoChoice, Inc.
EndoChoice, Inc. 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