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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Device
Medical Devices/Home Healthcare

HoMedics Air Compression Leg Massager Recalled for Packaging Errors

Agency Publication Date: August 28, 2025
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Summary

Zhejiang Luyao Electronics Technology Co., Ltd. has issued a voluntary recall for 3,705 units of the HoMedics Air Compression Leg Massager (Model SR-160HJ). The recall was initiated due to regulatory documentation errors and a misleading color claim on the product packaging. This massager is a powered inflatable garment used to temporarily relieve muscle aches and improve circulation in healthy adults.

Risk

The recall is due to administrative and labeling errors; the manufacturer has stated that the affected massagers do not present a risk of physical harm to users and no injuries have been reported.

What You Should Do

  1. This recall affects HoMedics Air Compression Leg Massagers (Model SR-160HJ) with UDI code 00031262108746. All lot numbers are included in this recall.
  2. Stop using the product.
  3. Return the product to the place of purchase for a refund or replacement, throw it away, or contact your healthcare provider or the manufacturer for further instructions.
  4. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) if you have additional questions regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider, or return the product to the place of purchase for a refund or replacement
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Stop using and throw the product away.

Affected Products

Product: Air Compression Leg Massagerby HOMEDICS
Model / REF:
SR-160HJ
Lot Numbers:
All lots (IRP)
UDI:
00031262108746

Product Code: IRP. Expiration Date: 2 YEARS.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97333
Status: Active
Manufacturer: Zhejiang Luyao Electronics Technology Co., Ltd.
Sold By: HoMedics
Manufactured In: China
Units Affected: 3705 US
Distributed To: Nationwide

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.