X-Pro Eagle 40cc Youth ATVs and FRP Sahara 40cc Youth ATVs
Summary
CPSC recall: X-Pro Eagle 40cc Youth ATVs and FRP Sahara 40cc Youth ATVs. By Yongkang Luyuan Industrial & Trading Co., Ltd., of China. Hazard: The recalled youth ATVs violate the mandatory ATV safety standard. The youth ATVs' mechanical suspension fails to comply with safety requirements, posing a crash hazard. Additionally, the handlebars pose a laceration hazard, if the child rider's body or head impacts the handlebars at high speed. ATVs that fail to meet the mandatory safety requirements pose
Details
Source
CPSC Consumer Product Recall
External ID
10524
Action Date
2025-12-11
Status
Recalled
Category
consumer_product
Product Description
This recall involves the X-Pro Eagle 40cc Youth ATV, Model CARTOONS and the FRP Sahara 40cc Youth ATV, Model SHR 40-RED-
Context & Analysis
This is a unclassified recall.
This was one of 18 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Yongkang Luyuan Industrial & Trading Co., Ltd., of China 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 Luyuan Industrial & Trading Co., Ltd., of China) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Yongkang Luyuan Industrial & Trading Co., Ltd., of China have FDA actions?
Yongkang Luyuan Industrial & Trading Co., Ltd., of China 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 "10524" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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