RecallHawk

Summary

CPSC recall: EGL and ACE-branded Youth All-Terrain Vehicles (ATVs). By AWL Distribution, BV Powersports, and other authorized dealerships nationwide from May 2020 through September 2020 for between $550 and $670.. Hazard: The ATVs fail to comply with the requirements of the federal mandatory ATV safety standard. The B125 ATVs exceed the maximum speed limitations for vehicles intended for children aged 10 and older. For the Madix 110, the parking brakes do not prevent the movement of the vehicle.

Details

Source

CPSC Consumer Product Recall

External ID

9269

Action Date

2022-03-24

Status

Recalled

Category

consumer_product

Product Description

The recall involves EGL and ACE-branded Youth ATVs, models MADIX 110 and B125. The vehicles were sold in various colors

Context & Analysis

This is a unclassified recall.

This was one of 8 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

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 (AWL Distribution, BV Powersports, and other authorized dealerships nationwide from May 2020 through September 2020 for between $550 and $670.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does AWL Distribution, BV Powersports, and other authorized dealerships nationwide from May 2020 through September 2020 for between $550 and $670. have FDA actions?

This is the only FDA action we have on record for AWL Distribution, BV Powersports, and other authorized dealerships nationwide from May 2020 through September 2020 for between $550 and $670. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9269" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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