RecallHawk

Peace Sports Youth All-Terrain Vehicles (ATVs)

Zhejiang Changying Car Industry Co. LTD, of China

Summary

CPSC recall: Peace Sports Youth All-Terrain Vehicles (ATVs). By Zhejiang Changying Car Industry Co. LTD, of China. Hazard: The youth ATVs fail to comply with the requirements of the federal mandatory ATV safety standard. The handlebars pose a laceration hazard if the child rider's body or head impacts the handlebars at a high rate of speed. Additionally, the parking brakes fail to hold, posing a collision hazard. The ATVs are also missing the required safety reflectors for vehicles intended for

Details

Source

CPSC Consumer Product Recall

External ID

10021

Action Date

2024-08-01

Status

Recalled

Category

consumer_product

Product Description

This recall involves Peace Industry Group "Peace Sports" 125CC Utility and Sport Youth ATVs with model numbers 512 CY125

Context & Analysis

This is a unclassified recall.

This was one of 20 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Zhejiang Changying Car Industry 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 (Zhejiang Changying Car Industry 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 Zhejiang Changying Car Industry Co. LTD, of China have FDA actions?

Zhejiang Changying Car Industry 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 "10021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for consumer_product

Related Actions