RecallHawk

Model Year 2024-2025 RZR XP 1000 and XP 4 1000 ROVs

Polaris Industries Inc., of Medina, Minnesota

Summary

CPSC recall: Model Year 2024-2025 RZR XP 1000 and XP 4 1000 ROVs. By Polaris Industries Inc., of Medina, Minnesota. Hazard: The positive (+) battery terminal cover (red) can become damaged by the seat base, causing the positive (+) battery post to be exposed and contact nearby conductive components, resulting in an electrical short, posing a fire hazard.. Remedy: Polaris is contacting all registered owners directly and providing a full-battery cover to them by mail that can be self-installed or

Details

Source

CPSC Consumer Product Recall

External ID

10106

Action Date

2024-12-05

Status

Recalled

Category

consumer_product

Product Description

This recall involves certain VINs of Polaris Model Year 2024-2025 RZR XP 1000 and XP 4 1000 ROVs. The recalled vehicles

Context & Analysis

This is a unclassified recall.

This was one of 8 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 "10106" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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