Air Compression Leg Massager Recall: HOMEDICS SR-160HJ
Announced 2025-09-03 · FDA
FDA recalls HOMEDICS Air Compression Leg Massager SR-160HJ for regulatory documentation error and misleading color packaging claim. All lots are affected; 3,705 units were distributed in the United States with worldwide distribution including Canada, and the notice states there is no risk of harm. No corrective action is listed.
| Brand | Zhejiang Luyao Electronics Technology Co., Ltd. |
|---|---|
| Product | Brand Name: HOMEDICS Product Name: Air Compression Leg Massager Model/Catalog Number: SR-160HJ Product Description: Powered Inflatable Tube Massager used on the leg. The Air Compression Leg Massager is indicated for the temporary relief of minor muscle aches and pains and for temporary increase in circulation to the treated areas in people who are in good health. The Air Compression Leg Massager simulates kneading and stroking of tissues by using an inflatable garment. |
| Reason | Regulatory documentation error and misleading color packaging claim. |
| Severity | moderate |
| Units affected | 3705 |
| Distribution | Worldwide distribution - US Nationwide and the country of Canada. |
| Agency | FDA |
| Recall / campaign no. | UDI: 00031262108746 Product Code: IRP Lot # : All lots affected, however they do not present risk of harm. Expiration Date: 2 YEARS |
WHAT YOU SHOULD DO
- Stop using the product immediately.
- Check if you own the recalled unit and note the recall details (UDI 00031262108746, Product Code IRP, model SR-160HJ).
- Contact Homedics customer service or the seller for instructions on return, replacement, or refund.
- Watch for updates from the FDA or the company about corrective actions.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.