Model Year 2023-2025 Ranger XP 1000 NorthStar and Ranger XP 1000 NorthStar Crew Recreational Off-Road Vehicles (ROVs)
Summary
CPSC recalled Model Year 2023-2025 Ranger XP 1000 NorthStar and Ranger XP 1000 NorthStar Crew Recreational Off-Road Vehicles (ROVs) by Polaris Industries Inc., of Medina, Minnesota. Hazard: The lower seat belt anchor fasteners were not properly tightened, which can result in the seat belt separating from the vehicle frame, failing to protect riders. Without that protection, riders can be ejected from the vehicle in a crash, posing an injury hazard.. Remedy: Consumers should immediately stop using the recalled ROVs and contact an authorized Polaris dealer to schedule a free inspection and repair at the dealer's location. Polaris advises that consumers may continue to operate the recalled ROVs prior to inspection and repair at the dealer, only if they conduct an inspection by following the Seat Belt Fastener Verification Instructions located on the firm's website. To continue operating the recalled ROVs prior to getting the repair, the fasteners must be secure where the seat belt anchor is attached to the vehicle frame. Polaris has contacted registered owners directly..
Details
Source
cpsc
External ID
25284
Action Date
2025-05-15
Status
Ongoing
Category
product
Product Description
This recall involves certain VINs of Polaris Model Year 2023-2025 Ranger XP 1000 NorthStar and Ranger XP 1000 NorthStar Crew ROVs. The recalled vehicles were sold in black, blue, brown, camouflage, gray, orange, red, tan 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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