FDA Recalls Two Unapproved Morning Life Air Compression Devices
Won Industry Co. is recalling two Morning Life air compression devices because they were distributed without FDA approval and have incorrect air compression settings.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, which typically corresponds to a moderate severity level where the use of the product may cause temporary or medically reversible health consequences. No specific injuries or illnesses are reported in the source text.
Plain-English summary
Won Industry Co. is voluntarily recalling two units of the Morning Life air compression device, models WIC2008S and WIC2008. The devices were distributed in Maryland, Texas, and Mexico.
The recall was initiated because the devices were distributed without FDA approval and have an incorrect air compression level setup. The devices are intended for limb massage to improve venous and lymphatic circulation.
Consumers who have these specific devices, identified by serial numbers EMM16100968 and EMM16100967, should stop using them and contact the recalling firm for instructions.
The recalled product
- 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
- Manufacturer
- Won Industry Co.
- Affected units
- 2
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Serial numbers: EMM16100968 and EMM16100967 MFG DATE: 2016.10.10
Distribution
Part of a larger recall action
This product is one of 2 recalled by Won Industry Co. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 2 products in this recall →Related recalls
Same manufacturer · Won Industry Co.
See all →- HighFDA Recalls Unapproved Compressible Limb Therapy Systems Due to Incorrect Air Compression
FDA (Devices) · 2017-12-13
Same hazard · unapproved device
See all →- ModerateCovidien esophageal stethoscope temperature sensors lack FDA clearance
FDA (Devices) · 2026-06-10
- ModerateCovidien 9 Fr Mon-a-Therm temperature probes lack FDA clearance
FDA (Devices) · 2026-06-10
- ModerateCovidien Mon-a-Therm general purpose temperature probes lack FDA clearance
FDA (Devices) · 2026-06-10
- ModerateOne Step 10A In Vitro Diagnostic Test Distributed Without FDA Clearance
FDA (Devices) · 2026-05-13
- ModerateOne Step K in vitro diagnostic test recall for missing FDA clearance
FDA (Devices) · 2026-05-13