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EndoChoice, Inc. recalls Fuse 1C Colonoscope
Recalled February 3, 2016 · FDA recall Z-0694-2016 · EndoChoice
Hazard
The bending section of the device may partially separate from the insertion tube. Potential for tissue trauma. · FDA Class II
Units
253 units
Sold at
Worldwide Distribution. US nationwide, Colombia, Denmark, France, Germany, Indonesia, Israel, Italy, Japan, Malaysia, Republic of Korea, Spain and Switzerland.
Description
The bending section of the device may partially separate from the insertion tube. Potential for tissue trauma.
Product
Fuse 1C Colonoscope
Manufacturer(s)
EndoChoice, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →