FDADecember 18, 2015device
Fuse 1C Colonoscope
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The bending section of the device may partially separate from the insertion tube. Potential for tissue trauma.
What to do
FDA enforcement status: Terminated
Brands named
endochoice
Recall history
No related federal recalls on record for this brand yet.
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