Model Years 2022-2024 Arctic Cat Prowler Pro / Pro Crew and Tracker Off Road 800SX / 800SX Crew Side by Side Recreationa
Summary
CPSC recalled Model Years 2022-2024 Arctic Cat Prowler Pro / Pro Crew and Tracker Off Road 800SX / 800SX Crew Side by Side Recreational Off Highway Vehicles (ROVs) by Textron Specialized Vehicles, of Augusta, Georgia. Hazard: The vehicle can move when on an incline and "park" is displayed on the digital dash. This can allow the vehicle to roll away, posing a crash hazard.. Remedy: Consumers should immediately stop using the recalled vehicles and contact Textron Specialized Vehicles to schedule a free repair. The repair kit will include a new shift cable bracket, shift sensor, and a decal to be placed at the dash display. The new shift sensor will allow the dash to display an "E" for shift error if "park" on the vehicle is not fully engaged. Customers will be directly notified to bring their vehicle to an authorized dealership to have the kit added at no cost. Textron is contacting all known purchasers directly..
Details
Source
cpsc
External ID
25701
Action Date
2024-10-17
Status
Ongoing
Category
product
Product Description
This recall involves all model years 2022, 2023 and 2024 Arctic Cat Prowler Pro and Pro Crew and all model year 2022, 2023 and 2024 Tracker Off Road 800SX and 800SX Crew Side by Side Recreational Off Highway Vehicles. The two-seat and four-seat vehicles were sold in various colors. The Arctic Cats have a "Prowler Pro" decal on the front hood and the Tracker Off Road vehicles have an "800SX" decal just outside the driver and passage doors.
Context & Analysis
Textron Specialized Vehicles, of Augusta, Georgia has 30 FDA actions in our database, including 15 recalls.
Frequently Asked Questions
How often does Textron Specialized Vehicles, of Augusta, Georgia have FDA actions?
Textron Specialized Vehicles, of Augusta, Georgia has 30 FDA actions in our database, including 15 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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