Model Year 2023-2024 Ranger XP Kinetic and Model Year 2025 Pro XD Kinetic ROVs
Summary
CPSC recalled 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 continue operating their vehicles until the repair can be completed. The instructions are available at https://www.polaris.com/en-us/recalls/off-road/polaris-recalls-some-model-year-2023-2024-ranger-xp-kinetic-and-model-year-2025-pro-xd-kinetic-vehicles.
Details
Source
cpsc
External ID
25343
Action Date
2025-06-18
Status
Ongoing
Category
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. The recalled Ranger XP Kinetic vehicles were sold in camouflage and white colors. The recalled Pro XD vehicles have gray plastic body panels with a black frame and accents. All vehicles were sold in three-seat configurations and have "POLARIS" stamped on the front grille. The VIN is printed on a portion of the left rear frame (on the driver's side of the vehicle) under the cargo box. In addition, this recall involves accessory charger service parts/kits with part numbers 2417296, 2417297, 2889704 and 2889486.
Context & Analysis
Polaris Industries Inc., of Medina, Minnesota has 56 FDA actions in our database, including 28 recalls.
Frequently Asked Questions
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. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.
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