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FDAFebruary 9, 2021device

In2Bones Shannon Percutaneous Burr - Product Usage: indicated for forefoot mini-invasive and percutaneous surgery.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

This Field Action is being conducted following identification of manufacturing non-conformity of some batches of Shannon burrs diameter 2.0mm length 20mm, possibly causing the breakage of the burr during use.

What to do

FDA enforcement status: Terminated

Brands named

in2bones sasin2bonesin2bones sas

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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In2Bones Shannon Percutaneous Burr - Product Usage: indicated for forefoot mini-invasive and percutaneous surgery. — Recall Details · AllClear