RecallHawk

XW-A17 Electric Youth All-Terrain Vehicles (ATVs)

Yongkang Ruihe Metal Products Co. Ltd., of China

Summary

CPSC recall: XW-A17 Electric Youth All-Terrain Vehicles (ATVs). By Yongkang Ruihe Metal Products Co. Ltd., of China. Hazard: The recalled youth ATVs violate the mandatory safety standard for ATVs because they are missing brake lights, reducing visibility of the youth ATV to other vehicles, posing a deadly crash hazard.. Remedy: Consumers should stop using the recalled youth ATVs immediately and contact Yamazuki for a free repair kit..

Details

Source

CPSC Consumer Product Recall

External ID

10832

Action Date

2026-06-25

Status

Recalled

Category

consumer_product

Product Description

This recall involves XW-A17 Electric Youth ATVs sold under brand names including Sunderwell in blue, green, orange and p

Context & Analysis

This is a unclassified recall.

This was one of 19 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Yongkang Ruihe Metal Products Co. Ltd., of China has 4 FDA actions in our database, including 2 recalls.

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 Ruihe Metal Products 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 Ruihe Metal Products Co. Ltd., of China have FDA actions?

Yongkang Ruihe Metal Products Co. Ltd., of China has 4 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "10832" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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