RecallHawk

Model Year 2024 RANGER XD 1500 and Crew XD 1500 Recreational Off-Road Vehicles (ROVs)

Polaris Industries Inc., of Medina, Minnesota

Summary

CPSC recall: Model Year 2024 RANGER XD 1500 and Crew XD 1500 Recreational Off-Road Vehicles (ROVs). By Polaris Industries Inc., of Medina, Minnesota. Hazard: The winch wiring can overheat while in use, posing a fire hazard and risk of serious injury to the rider or passenger.. Remedy: Consumers should immediately stop using the winch in the recalled ROVs and contact an authorized Polaris dealer to schedule a free repair to confirm a proper winch ground connection at the dealer's location. Polari

Details

Source

CPSC Consumer Product Recall

External ID

10058

Action Date

2024-09-19

Status

Recalled

Category

consumer_product

Product Description

This recall involves certain VINs of Polaris Model Year 2024 RANGER XD 1500 and RANGER CREW XD 1500 ROVs. The recalled R

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.

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 "10058" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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