RecallHawk

Arctic Cat Alterra 600 and Tracker 600 All-Terrain Vehicles (ATVs)

Textron Specialized Vehicles, of Augusta, Georgia

Summary

CPSC recall: Arctic Cat Alterra 600 and Tracker 600 All-Terrain Vehicles (ATVs). By Textron Specialized Vehicles, of Augusta, Georgia. Hazard: A fuse in the ATV's electrical system can fail during operation, which can result in sudden loss of engine power and headlights, posing a crash hazard.. Remedy: Consumers should immediately stop using the recalled ATVs and contact Textron Specialized Vehicles to arrange for a free repair. Textron will send consumers instructions along with a replacement

Details

Source

CPSC Consumer Product Recall

External ID

9365

Action Date

2022-07-28

Status

Recalled

Category

consumer_product

Product Description

This recall involves model year 2022 Arctic Cat Alterra 600 and model year 2022 Tracker 600 All-Terrain Vehicles (ATVs).

Context & Analysis

This is a unclassified recall.

This was one of 15 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Textron Specialized Vehicles, of Augusta, Georgia has 30 FDA actions in our database, including 15 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 (Textron Specialized Vehicles, of Augusta, Georgia) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Textron Specialized Vehicles, of Augusta, Georgia have FDA actions?

Textron Specialized Vehicles, of Augusta, Georgia has 30 FDA actions in our database, including 15 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9365" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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