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.
FDA Recall Z-2880-2018 · Posted None
Recalling FirmIn2bones USA, LLC
Recall StatusTerminated
Product CodeHWC
Date Initiated2018-07-16
Date Terminated2019-02-22
Product Quantity48 units
Reason for Recall
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.
Firm Action
In2Bones sent a Medical Device Recall letter dated July 18, 2018 to affected customers (agents and hospitals). The letter identified the affected product, problem and actions to be taken. The Agent notice requested the consignee to inform and distribute the notice to all relevant person within the organization. The firm is seeking the return of the products
The notice to the hospitals and healthcare professionals explained the problem and recommended that patients be monitored for any adverse events within the normal standard of practice.
For questions contact Quality and Regulatory Affairs Team at 901-260-7931..
Root Cause
Process control
Distribution Pattern
Worldwide Distribution - US Nationwide and the countries of France
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.