Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CoLink(TM) Lapidus Plate XP Recalled by In2bones USA, LLC Due to CoLink(TM) Lapidus Plate +2mm Right and Left, were...
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 In2bones USA, LLC directly.
Affected Products
CoLink(TM) Lapidus Plate XP, +2 mm, Left, REF P40 ST265, QTY 1, In2Bones Product Usage: The In2Bones USA LLC, CoLink¿ Plating System is indicated for stabilization and fixation of fractures, revision procedures, joint fusion, osteotomies and reconstruction of the small bones in the hand, wrist, foot and ankle in both pediatric and adult patients.
Quantity: 48 units
Why Was This Recalled?
CoLink(TM) Lapidus Plate +2mm Right and Left, were laser marked incorrectly. In these lots, right plates were laser marked as left plates and the left plates were laser marked as right plates.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About In2bones USA, LLC
In2bones USA, LLC has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report