# FDA recall Z-0204-2018

> **Won Industry Co.** · Class II · device recall initiated 2017-01-13.

## Product

Morning Life, Model WIC2008S & WIC2008, UDI 8809293 870336    Product Usage:  Intended for limb massage utilizing air compression. It is specially designed to improve venous and lymphatic circulation by compressing and releasing air pressure programmed on the device. It helps to prevent the blood blockage in cardiovascular and to relax stressed muscle by increasing the temperature of hypodermic tissue and expanding the blood vessels. It vitalizes the circulation of blood and lymph in arms, legs and waist and enhances the pressure of muscular issues to remove swelling or pain.

## Reason for recall

Distribution of unapproved devices with incorrect air compression level setup

## Distribution

Worldwide distribution - US Nationwide - Domestic: MD & TX; Internationally: Mexico

## Key facts

- **Recall number:** Z-0204-2018
- **Recalling firm:** Won Industry Co.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-01-13
- **Report date:** 2017-12-13
- **Termination date:** 2023-05-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Siheung-si, N/A, Korea (the Republic of)

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0204-2018

## Citation

> AI Analytics. FDA recall Z-0204-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0204-2018. Source: US FDA. Licensed CC0.

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