RecallHawk

Can-Am Outlander Pro and Max Pro All-Terrain Vehicles

Unknown Manufacturer

Summary

CPSC recalled Can-Am Outlander Pro and Max Pro All-Terrain Vehicles by Unknown Manufacturer. Hazard: The ATV's speed limiter control can malfunction, causing unexpected speed and acceleration, posing a serious risk of injury or death from crash hazard.. Remedy: Consumers should stop using the Speed Limiter Mode immediately and contact an authorized Can-Am Off-Road dealer to schedule a free repair at the dealership, involving a software update that will take less than one hour. To find an authorized dealer visit https://can-am.brp.com/off-road/us/en/find-a-dealer.html#/search..

Details

Source

cpsc

External ID

26482

Action Date

2026-05-14

Status

Ongoing

Category

product

Product Description

This recall involves model years 25 and 26 Can-Am Outlander 500 or 700 Pro and Max Pro ATVs equipped with Speed Limiter Mode and model years 23 and 24 Can-Am Outlander Pro and Max Pro ATVs equipped with Speed Limiter Mode that received an Engine Control Module (ECM) software update at a dealership on or after February 3, 2026. The ATVs were sold in Tan, Green, Camo and Gray. The model year (MY) can be identified by the 10th character of the vehicle's 17-digit Vehicle Identification Number (VIN). P = 2023, R = 2024, S = 2025, T = 2026. The VIN label is located on the front right side of the vehicle, on the frame. The stamped VIN is located on the front member on the right side of the vehicle. The model name "OUTLANDER PRO" is displayed on the vehicle's front side and the 'Can?Am' branding is located on the left rear fender near the tail section.

Context & Analysis

Unknown Manufacturer has 1320 FDA actions in our database.

Frequently Asked Questions

How often does Unknown Manufacturer have FDA actions?

Unknown Manufacturer has 1320 FDA actions in our database, including 0 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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