RecallHawk

Arctic Cat 8000 and 9000 Series Snowmobiles

Arctic Cat, of Thief River Falls, Minnesota

Summary

CPSC recall: Arctic Cat 8000 and 9000 Series Snowmobiles. By Arctic Cat, of Thief River Falls, Minnesota. Hazard: The recalled snowmobile's drive clutch can break, allowing fragments to escape the snowmobile shielding, posing a laceration hazard.. Remedy: Consumers should immediately stop using the recalled snowmobiles, and contact Arctic Cat to schedule for a free installation of an additional clutch guard and inspection of the primary clutch. If the primary clutch is cracked, Arctic Cat will r

Details

Source

CPSC Consumer Product Recall

External ID

9944

Action Date

2024-05-02

Status

Recalled

Category

consumer_product

Product Description

This recall involves all model year 2017-2021 Arctic Cat 8000 and 9000 series snowmobiles, and certain model year 2022 A

Context & Analysis

This is a unclassified recall.

This was one of 16 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Arctic Cat, of Thief River Falls, Minnesota has 2 FDA actions in our database, including 1 recall.

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 (Arctic Cat, of Thief River Falls, Minnesota) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Arctic Cat, of Thief River Falls, Minnesota have FDA actions?

Arctic Cat, of Thief River Falls, Minnesota has 2 FDA actions in our database, including 1 recall and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9944" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for consumer_product

Related Actions