# FDA recall Z-1366-2022

> **Wright Medical Technology, Inc.** · Class II · device recall initiated 2022-06-14.

## Product

Wright EVOLVE TRIAD Plate Cutter, REF 49510120

## Reason for recall

The plate cutter is unable to meet sterilization requirements when it is sterilized in a double-wrapped configuration according to the Option 1 Steam Sterilization parameters detailed in instructions for use

## Distribution

Nationwide and PR, and Australia, Canada, Chile, Colombia, Hong Kong, Puerto Rico

## Key facts

- **Recall number:** Z-1366-2022
- **Recalling firm:** Wright Medical Technology, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-06-14
- **Report date:** 2022-07-20

- **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-1366-2022

## Citation

> AI Analytics. FDA recall Z-1366-2022. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1366-2022. Source: US FDA. Licensed CC0.

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