RecallHawk

Model Year 2025 Ski-Doo and Lynx snowmobiles equipped with a 600R E-TEC, 850 E-TEC or 850 E-TEC Turbo R engine

Bombardier Recreational Products Inc., of Canada

Summary

CPSC recalled Model Year 2025 Ski-Doo and Lynx snowmobiles equipped with a 600R E-TEC, 850 E-TEC or 850 E-TEC Turbo R engine by Bombardier Recreational Products Inc., of Canada. Hazard: The engine control module (ECM) lower mount support could have broken in production and left a loose part inside the engine compartment, allowing it to enter the throttle body area and lead to a stuck throttle. This poses a crash hazard and risk of serious injuries or death.. Remedy: Consumers should immediately stop using the recalled snowmobiles and contact a BRP dealer to schedule a free appointment. Dealers will inspect the ECM and the throttle body area to look for any ECM lower mount support broken part. If found, dealers will remove the detached part and replace the ECM free of charge. BRP is contacting all known purchasers..

Details

Source

cpsc

External ID

25188

Action Date

2025-03-20

Status

Ongoing

Category

product

Product Description

This recall involves certain Model Year 2025 Ski-Doo and Lynx snowmobiles equipped with a 600R E-TEC, a 850 E-TEC or a 850 E-TEC Turbo R engine. The brand name "Ski-Doo," the model name and engine type are printed on the side panels of the vehicles. The vehicle identification number (VIN) is on the decal located on the right-hand side of the tunnel underneath the seat. Dealers can check for VINs included in this recall. The snowmobiles were sold in various color combinations.

Context & Analysis

Bombardier Recreational Products Inc., of Canada has 8 FDA actions in our database, including 4 recalls.

Frequently Asked Questions

How often does Bombardier Recreational Products Inc., of Canada have FDA actions?

Bombardier Recreational Products Inc., of Canada has 8 FDA actions in our database, including 4 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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