Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported December 13, 2017
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
Distribution of unapproved devices with incorrect air compression level setup
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Won Industry Co. recalled Morning Life, Model WIC2008S & WIC2008, UDI 8809293 870336 Product Usage: Intended fo… - a moderate-severity action.
Morning Life, Model WIC2008S & WIC2008, UDI 8809293 870336 Product Usage: Intended fo… was recalled by Won Industry Co. in December 13, 2017. Reason: Distribution of unapproved devices with incorrect air compression level setup. Check the official notice for the remedy. Verify recall #Z-0204-2018 with the FDA Devices before acting.
The recall
Won Industry Co. issued this moderate-severity FDA Devices recall-Distribution of unapproved devices with incorrect air compression level setup.
- Moderate
- severity level
- 2 units
- affected scope
- Class II
- classification
- December 13, 2017
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0204-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0204-2018) was formally reported on December 13, 2017, with the manufacturer initiating the action on January 13, 2017. It is classified under Moderate severity (Class II), with a current status of Terminated. Won Industry Co. is listed as the recalling firm, operating out of Siheung-si, N/A. Federal records list the affected scope as 2.
The documented reason for this recall is: Distribution of unapproved devices with incorrect air compression level setup Distribution data in the federal record shows the product reached: Worldwide distribution - US Nationwide - Domestic: MD & TX; Internationally: Mexico. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,422 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
2
Related Recalls
6
0 from same agency
Product description
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
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0204-2018 |
| Date reported | December 13, 2017 |
| Date initiated | January 13, 2017 |
| Recalling firm | Won Industry Co. |
| Firm location | Siheung-si, N/A |
| Affected scope | 2 |
| Distribution | Worldwide distribution - US Nationwide - Domestic: MD & TX; Internationally: Mexico |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-0204-2018) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Won Industry Co.. Units affected: 2.
Why was this product recalled? ▼
Distribution of unapproved devices with incorrect air compression level setup
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 13, 2017. Severity: Moderate. Recall number: Z-0204-2018.
Where was the recalled product distributed? ▼
Distribution: Worldwide distribution - US Nationwide - Domestic: MD & TX; Internationally: Mexico.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0204-2018) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported December 13, 2017. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.