# FDA recall Z-2880-2018

> **In2bones USA, LLC** · Class II · device recall initiated 2018-07-16.

## Product

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.

## 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.

## Distribution

Worldwide Distribution - US Nationwide and the countries of France

## Key facts

- **Recall number:** Z-2880-2018
- **Recalling firm:** In2bones USA, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-07-16
- **Report date:** 2018-08-29
- **Termination date:** 2019-02-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Memphis, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2880-2018

## Citation

> AI Analytics. FDA recall Z-2880-2018. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-2880-2018. Source: US FDA. Licensed CC0.

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