EGL and ACE Branded Youth All-Terrain Vehicles (ATVs)
Yongkang Jiayue Industry & Trading Co., Ltd., of China (model D110)
Summary
CPSC recall: EGL and ACE Branded Youth All-Terrain Vehicles (ATVs). By Yongkang Jiayue Industry & Trading Co., Ltd., of China (model D110). Hazard: The youth ATVs fail to comply with the requirements of the federal mandatory ATV safety standard. Children can operate them above the maximum allowed speed, increasing the risk of a crash that can cause serious injuries. The handlebars pose a laceration hazard should the child rider's body or head impact the handlebars at a high rate of speed such as
Details
Source
CPSC Consumer Product Recall
External ID
9207
Action Date
2022-01-12
Status
Recalled
Category
consumer_product
Product Description
The recall involves EGL and ACE branded Youth ATVs, models MADIX 125 and D110. The name of the vehicle is printed on a l
Context & Analysis
This is a unclassified recall.
This was one of 10 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Yongkang Jiayue Industry & Trading Co., Ltd., of China (model D110) has 2 FDA actions in our database, including 1 recall.
Frequently Asked Questions
What is a FDA recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Yongkang Jiayue Industry & Trading Co., Ltd., of China (model D110)) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Yongkang Jiayue Industry & Trading Co., Ltd., of China (model D110) have FDA actions?
Yongkang Jiayue Industry & Trading Co., Ltd., of China (model D110) has 2 FDA actions in our database, including 1 recall and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9207" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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