RecallHawk

Model Year 2022 MATRYX RMK, INDY, SWITCHBACK, VOYAGEUR, and NORDIC PRO snowmobiles

Polaris Industries Inc., of Medina, Minnesota

Summary

CPSC recall: Model Year 2022 MATRYX RMK, INDY, SWITCHBACK, VOYAGEUR, and NORDIC PRO snowmobiles. By Polaris Industries Inc., of Medina, Minnesota. Hazard: The throttle release switch (TRS) can fail to disengage when the throttle lever is released and if a stuck throttle condition occurs when the TRS fails to disengage, it can lead to loss of vehicle control, posing a crash hazard. Additionally, on certain Model Year 2022 MATRYX RMK snowmobiles, the throttle cable can be kinked during installatio

Details

Source

CPSC Consumer Product Recall

External ID

9246

Action Date

2022-02-17

Status

Recalled

Category

consumer_product

Product Description

This recall involves certain VINs of Model Year 2022 MATRYX RMK, INDY, SWITCHBACK, VOYAGEUR, and NORDIC PRO snowmobiles.

Context & Analysis

This is a unclassified recall.

This was one of 18 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Polaris Industries Inc., of Medina, Minnesota has 56 FDA actions in our database, including 28 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 (Polaris Industries Inc., of Medina, Minnesota) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Polaris Industries Inc., of Medina, Minnesota have FDA actions?

Polaris Industries Inc., of Medina, Minnesota has 56 FDA actions in our database, including 28 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9246" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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