RecallHawk

Model Year 2023 PATRIOT 9R MATRYX PRO RMK and PATRIOT 9R MATRYX RMK KHAOS Snowmobiles

Polaris Industries Inc., of Medina, Minnesota

Summary

CPSC recall: Model Year 2023 PATRIOT 9R MATRYX PRO RMK and PATRIOT 9R MATRYX RMK KHAOS Snowmobiles. By Polaris Industries Inc., of Medina, Minnesota. Hazard: The primary (drive) clutch can fail and can cause the clutch or clutch components to come loose, posing an injury hazard to consumers.. Remedy: Consumers should immediately stop using the recalled snowmobiles and contact Polaris or an authorized Polaris dealer to schedule a free repair to replace the primary (drive) clutch, install a clutch

Details

Source

CPSC Consumer Product Recall

External ID

9774

Action Date

2023-11-30

Status

Recalled

Category

consumer_product

Product Description

This recall involves Polaris Model Year 2023 PATRIOT 9R MATRYX PRO RMK and PATRIOT 9R MATRYX RMK KHAOS. The recalled sno

Context & Analysis

This is a unclassified recall.

This was one of 11 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 "9774" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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