RecallHawk

Fugleman® UT10E and UT10X Utility Terrain Vehicles (UTVs)

Segway Technology Co. Ltd., of China

Summary

CPSC recall: Fugleman® UT10E and UT10X Utility Terrain Vehicles (UTVs). By Segway Technology Co. Ltd., of China. Hazard: The cockpit rear panel between the seats and the cargo bed can overheat and melt the plastic, 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 installation of larger and additional heat shields. The firm has contacted all known purchasers.

Details

Source

CPSC Consumer Product Recall

External ID

9350

Action Date

2022-07-07

Status

Recalled

Category

consumer_product

Product Description

This recall involves model year 2022 Fugleman UT10E and UT10X Utility Terrain Vehicles (UTVs). These vehicles were sold

Context & Analysis

This is a unclassified recall.

This was one of 10 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 "9350" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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