Ricky Powersports Youth All-Terrain Vehicles (ATVs)
Zhejiang Guoyu Industry & Trading Co. Ltd., of Zhejiang, China
Summary
CPSC recall: Ricky Powersports Youth All-Terrain Vehicles (ATVs). By Zhejiang Guoyu Industry & Trading Co. Ltd., of Zhejiang, China. Hazard: The recalled ATVs fail to comply with the mandatory requirements of the federal ATV safety standard, including parking brake requirements, posing a collision hazard to consumers if the vehicle is parked on an incline. The ATVs also fail to comply with other mandatory safety requirements for ATVs intended for children 10 years of age and older, including imp
Details
Source
CPSC Consumer Product Recall
External ID
9612
Action Date
2023-05-04
Status
Recalled
Category
consumer_product
Product Description
The recall involves Ricky Powersports RPS Youth BF-ATV125E 125cc ATVs. The ATVs were sold in burgundy, purple camo, red
Context & Analysis
This is a unclassified recall.
This was one of 15 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Zhejiang Guoyu Industry & Trading Co. Ltd., of Zhejiang, 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 (Zhejiang Guoyu Industry & Trading Co. Ltd., of Zhejiang, China) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Zhejiang Guoyu Industry & Trading Co. Ltd., of Zhejiang, China have FDA actions?
Zhejiang Guoyu Industry & Trading Co. Ltd., of Zhejiang, 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 "9612" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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