# FDA recall Z-1567-2022

> **Wright Medical Technology, Inc.** · Class II · device recall initiated 2022-07-27.

## Product

Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00, REF 4700020, Sterile.

## Reason for recall

An incorrect sizing label was applied to the carton packaging.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of AZ, CA, FL, GA, NY, PA, and TN. The countries of the Australia, France, the Netherlands, Sweden, and the United Kingdom.

## Key facts

- **Recall number:** Z-1567-2022
- **Recalling firm:** Wright Medical Technology, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-07-27
- **Report date:** 2022-08-31

- **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-1567-2022

## Citation

> AI Analytics. FDA recall Z-1567-2022. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1567-2022. Source: US FDA. Licensed CC0.

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