Model Year 2025-2026 Ranger XP 1000 NorthStar and Ranger Crew XP 1000 NorthStar Recreational Off-Road Vehicles (ROVs)
Summary
CPSC recalled Model Year 2025-2026 Ranger XP 1000 NorthStar and Ranger Crew XP 1000 NorthStar Recreational Off-Road Vehicles (ROVs) by Polaris Industries Inc., of Medina, Minnesota. Hazard: An improperly routed alternator cable can become damaged and contact the negative battery post, resulting in an electrical short, posing a fire hazard and risk of serious injury.. Remedy: Consumers should immediately stop using the recalled ROVs and go to https://www.polaris.com/en-us/recalls/off-road/polaris-recalls-some-model-year-2025-2026-ranger-xp-1000-and-crew-xp-1000-vehicles/ to determine if their vehicle falls under the scope of the recall. Polaris is providing instructions on how to continue operating their vehicles until the repair can be completed or to contact an authorized Polaris dealer to schedule a free repair at the dealer's location..
Details
Source
cpsc
External ID
26054
Action Date
2025-10-30
Status
Ongoing
Category
product
Product Description
This recall involves certain VINs of Polaris Model Year 2025-2026 Ranger XP 1000 NorthStar and Ranger Crew XP 1000 NorthStar ROVs. The recalled vehicles were sold in black, blue, bronze, brown, camouflage, gray, orange, red and white. The vehicles were sold in three and six-seat configurations and have "POLARIS" stamped on the front grille. The VIN is printed on the left rear frame (on the driver's side of the vehicle) under the cargo box.
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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