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 recall: 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

Details

Source

CPSC Consumer Product Recall

External ID

10206

Action Date

2025-03-20

Status

Recalled

Category

consumer_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 8

Context & Analysis

This is a unclassified recall.

This was one of 18 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

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

Frequently Asked Questions

What is a FDA recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Bombardier Recreational Products Inc., of Canada) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

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. Search for "10206" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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