# FDA recall Z-1291-2022

> **Wright Medical Technology, Inc.** · Class II · device recall initiated 2022-06-02.

## Product

Stryker INFINITY Resect Guide for INBONE Talus, Size 4, Model #33620254, non-sterile, an instrument used with the INFINITY Total Ankle System.

## Reason for recall

The instrument is incorrectly color coded.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of AZ, CA, CO, CT, FL, GA, IA, IL, MA, MI, MN, MO, NC, NY, OH, PA, TX, and WA.  The countries of Australia, Belgium, Canada, France, Germany, Hong Kong, Israel, Sweden, Switzerland, and United Kingdom.

## Key facts

- **Recall number:** Z-1291-2022
- **Recalling firm:** Wright Medical Technology, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-06-02
- **Report date:** 2022-07-06

- **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-1291-2022

## Citation

> AI Analytics. FDA recall Z-1291-2022. Retrieved 2026-06-10 from https://api.ai-analytics.org/recall/Z-1291-2022. Source: US FDA. Licensed CC0.

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