RecallHawk

E-Bully Youth All-Terrain Vehicles (ATVs)

Shandong ODES Industry Co. Ltd., of China

Summary

CPSC recall: E-Bully Youth All-Terrain Vehicles (ATVs). By Shandong ODES Industry Co. Ltd., of China. Hazard: The recalled 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. ATVs that fail to meet the mandatory safety requirements pose a risk of serious injury

Details

Source

CPSC Consumer Product Recall

External ID

10234

Action Date

2025-04-10

Status

Recalled

Category

consumer_product

Product Description

This recall involves the E-Bully Youth Electric 1000W ATVs sold under various brand names, including "Seangles" and "Off

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.

Shandong ODES 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 (Shandong ODES 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 Shandong ODES Industry Co. Ltd., of China have FDA actions?

Shandong ODES 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 "10234" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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