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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 78182

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
January 13, 2017
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Won Industry Co.

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 2

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
Recall number
Z-0204-2018
Initiated
January 13, 2017
Classification
Class II
Status
Terminated
Recalling firm
Won Industry Co.
Quantity
2

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Distribution of unapproved devices with incorrect air compression level setup

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

device · product 2 of 2

Compressible Limb Therapy System (Leg Cuffs, Arm Sleeves, Waist pads and air injection hoses) 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-0205-2018
Recall number
Z-0205-2018
Initiated
January 13, 2017
Classification
Class II
Status
Terminated
Recalling firm
Won Industry Co.
Quantity
3

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Distribution of unapproved devices with incorrect air compression level setup

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Distribution of unapproved devices with incorrect air compression level setup

Code information

none

Distribution pattern

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