HOMEDICS Air Compression Leg Massager recall — FDA Z-2463-2025
Regulatory documentation error and misleading color packaging claim.
Overview of recall records associated with Zhejiang Luyao Electronics Technology Co., Ltd., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Regulatory documentation error and misleading color packaging claim.
This page summarizes recall records in which the official source identifies Zhejiang Luyao Electronics Technology Co., Ltd. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.