# FDA recall Z-0786-2022

> **Wright Medical Technology, Inc.** · Class II · device recall initiated 2022-02-15.

## Product

Wright Medical Technology, Inc. ORTHOLOC Non-Locking Screw 2mm x 8mm, REF 5201120008, non-sterile, a component of the ORTHOLOC 2.0/2.4 Plate System.

## Reason for recall

An incorrect screw is packaged in the product, which contains a locking screw instead of a non-locking screw.

## Distribution

International distribution to the country of France.

## Key facts

- **Recall number:** Z-0786-2022
- **Recalling firm:** Wright Medical Technology, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-02-15
- **Report date:** 2022-03-23
- **Termination date:** 2022-10-05

- **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-0786-2022

## Citation

> AI Analytics. FDA recall Z-0786-2022. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/Z-0786-2022. Source: US FDA. Licensed CC0.

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