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Recall Observatory FDA recall evidence

Device 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.

Z-0204-2018

January 13, 2017

Class II

Product summary

Firm
Won Industry Co.
Event
Event 78182
Status
Terminated
Classification
Class II
Quantity
2
Official record key
device-enforcement:Z-0204-2018

Official wording

Reason: Distribution of unapproved devices with incorrect air compression level setup

Code information: Serial numbers: EMM16100968 and EMM16100967 MFG DATE: 2016.10.10

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

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Distribution of unapproved devices with incorrect air compression level setup