RecallHawk

2022 Fugleman UT10E and UT10X Utility-Terrain Vehicles

Segway Technology Co. Ltd., of China

Summary

CPSC recall: 2022 Fugleman UT10E and UT10X Utility-Terrain Vehicles. By Segway Technology Co. Ltd., of China. Hazard: The ignition coil can fail to ignite one of the engine cylinders, allowing uncombusted fuel to enter the exhaust pipe where it could ignite, posing a fire hazard.. Remedy: Consumers should immediately stop using the recalled UTVs and bring the vehicles to an authorized Segway Powersports dealer for a free repair, which includes the installation of an upgrade kit. The firm has con

Details

Source

CPSC Consumer Product Recall

External ID

9789

Action Date

2023-12-07

Status

Recalled

Category

consumer_product

Product Description

This recall involves model year 2022 Fugleman Utility -Terrain Vehicles (UTVs) with model numbers UT10E or UT10X. These

Context & Analysis

This is a unclassified recall.

This was one of 26 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Segway Technology 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 (Segway Technology 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 Segway Technology Co. Ltd., of China have FDA actions?

Segway Technology 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 "9789" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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