# FDA recall Z-1102-2020

> **Wright Medical Technology, Inc.** · Class II · device recall initiated 2019-12-27.

## Product

WRIGHT EVOLVE Proline Head, Size: +2, OD: 22mm, REF 496H222

## Reason for recall

Two lots of EVOLVE Modular Radial Head could have the wrong size product in the package.  Both the label and laser marking are incorrect on the affected product.

## Distribution

US

## Key facts

- **Recall number:** Z-1102-2020
- **Recalling firm:** Wright Medical Technology, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-12-27
- **Report date:** 2020-02-12
- **Termination date:** 2021-07-23

- **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-1102-2020

## Citation

> AI Analytics. FDA recall Z-1102-2020. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1102-2020. Source: US FDA. Licensed CC0.

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