# FDA recall Z-0679-2022

> **Wright Medical Technology, Inc.** · Class II · device recall initiated 2022-02-09.

## Product

The DARCO¿ Locking Bone Plate System is designed with rhombus  (parallelogram) plates of biocompatible titanium. The plates use either 2.7mm or  3.5mm screws which intersect each other in pairs. The drill holes of the plates are  aligned to assure the screws do not touch. The various plates model numbers differ  from each other through among other things different curvatures, material  strengths, lengths, number of plate holes and through different grades and bridge  widths

## Reason for recall

Product was labelled with the incorrect manufacturing and distribution dates.

## Distribution

International distribution in the countries of Japan and the United Kingdom.

## Key facts

- **Recall number:** Z-0679-2022
- **Recalling firm:** Wright Medical Technology, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-02-09
- **Report date:** 2022-03-09
- **Termination date:** 2024-01-25

- **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-0679-2022

## Citation

> AI Analytics. FDA recall Z-0679-2022. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-0679-2022. Source: US FDA. Licensed CC0.

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