In2Bones, SAS 28 Chemin du petit Bois Ecully France In2Bones Shannon Percutaneous Burr - Product Usage: indicated for forefoot mini-invasive and percutaneous surgery. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
In2Bones Shannon Percutaneous Burr - Product Usage: indicated for forefoot mini-invasive and percutaneous surgery.
Brand
In2Bones, SAS 28 Chemin du petit Bois Ecully France
Lot Codes / Batch Numbers
Model G01 01511, Batches 2009139 and 2001089 Model G01 01512, Batches 2007087 and 2011062
Products Sold
Model G01 01511, Batches 2009139 and 2001089 Model G01 01512, Batches 2007087 and 2011062
In2Bones, SAS 28 Chemin du petit Bois Ecully France is recalling In2Bones Shannon Percutaneous Burr - Product Usage: indicated for forefoot mini-invasive and percut due to This Field Action is being conducted following identification of manufacturing non-conformity of some batches of Shannon burrs diameter 2.0mm length 2. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
A "FIELD CORRECTIVE ACTION MEDICAL DEVICE BATCH RECALL" and reply form dated 02/09/2021 were sent to customers.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026