In2bones recalls one unit of CoLink Lapidus Plate XP +2mm Right (REF P40 ST1:165) due to incorrect laser marking. This could lead to improper use in orthopedic procedures.
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.
In2bones is recalling one specific unit of their CoLink Lapidus Plate XP +2mm Right plate because it was laser marked incorrectly. This error could cause improper use during orthopedic procedures if the plate is used without careful verification.
The laser marking on the plate was swapped between left and right sides. This could lead to using the wrong plate side during surgery, potentially causing improper fixation of fractures or joint issues.
Orthopedic surgeons and patients using the CoLink Lapidus Plate XP +2mm Right (REF P40 ST165) for hand, wrist, foot, or ankle procedures. Those most at risk are users who might not verify the plate's marking.
Check for the product name 'CoLink Lapidus Plate XP +2 mm Right', reference number P40 ST165, and lot number 1704073. This specific unit was recalled due to incorrect laser marking.
Check if the plate is laser marked as a right plate but labeled as left, or vice versa.
The CoLink Lapidus Plate XP +2mm Right was laser marked incorrectly, swapping left and right markings.
One unit (reference P40 ST165, lot 1704073) was recalled.
The recall record does not specify a remedy, so no fix is provided.
We’ve drafted a message you can send In2bones to request your refund or repair — edit it as you like.
Subject: Recall Z-2879-2018 — In2bones In2bones Hello, I own a In2bones that is covered by recall Z-2879-2018 from In2bones. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.