RecallHawk

EGL Motor ACE-branded Youth All-Terrain Vehicles (ATVs)

Unknown Manufacturer

Summary

CPSC recalled EGL Motor ACE-branded Youth All-Terrain Vehicles (ATVs) by Unknown Manufacturer. Hazard: The recalled ATVs fail to comply with the requirements of the federal mandatory ATV safety standard. The Ace-branded K125 and C125 models exceed the maximum speed limitations for vehicles intended for children aged 10 and older, posing a risk of high-speed crash. For T125 and C125 models, the parking brakes do not prevent movement of the vehicle, posing a collision hazard to consumers if the vehicle is parked on an incline. ATVs that fail to meet the mandatory safety requirements pose a risk of serious injury or death.. Remedy: Consumers should immediately stop using the recalled ATVs and contact EGL Motor to schedule an appointment for a free repair from an authorized repair shop. The firm will repair reflectors, headlights, chest protector, engine stop switch, parking brake, maximum speeds, and spark arrestor on the recalled models..

Details

Source

cpsc

External ID

23191

Action Date

2023-04-27

Status

Ongoing

Category

product

Product Description

The recall involves EGL Motor's ACE-branded Youth ATVs, models K125, T125 and C125. The vehicles were sold in various colors including orange, red, blue, pink and green and marketed for children ages 10 and older. The model name "ACE POWER K125," "ACE POWER T125" or "ACE POWER CONQUEROR" is displayed on both sides of the vehicle. The model number is stamped into the metal plate located on the left side, under the rear body. The phrase "This ATV is subject to EGL MOTOR INC's action plan approved by U.S. Consumer Product Safety Commission" is printed on a label located under the model number plate.

Context & Analysis

Unknown Manufacturer has 1320 FDA actions in our database.

Frequently Asked Questions

How often does Unknown Manufacturer have FDA actions?

Unknown Manufacturer has 1320 FDA actions in our database, including 0 recalls and 0 device clearances.

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The official record is available on FDA.gov. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.

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