RecallHawk

Model Year 2023-2024 Ranger XP Kinetic and Model Year 2025 Pro XD Kinetic ROVs

Polaris Industries Inc., of Medina, Minnesota

Summary

CPSC recall: Model Year 2023-2024 Ranger XP Kinetic and Model Year 2025 Pro XD Kinetic ROVs. By Polaris Industries Inc., of Medina, Minnesota. Hazard: Water can leak through a cracked filter into the ROV's high-voltage charging harness components and cause a short circuit, posing a fire hazard.. Remedy: Consumers should contact an authorized Polaris dealer to schedule a free repair at the dealer's location. Polaris is contacting all registered owners directly and providing instructions on how to

Details

Source

CPSC Consumer Product Recall

External ID

10315

Action Date

2025-06-18

Status

Recalled

Category

consumer_product

Product Description

This recall involves all VINs of Polaris Model Year 2023-2024 Ranger XP Kinetic and Model Year 2025 Pro XD Kinetic ROVs.

Context & Analysis

This is a unclassified recall.

This was one of 12 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 "10315" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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