Ski-Doo snowmobiles
Ski-Doo dealers nationwide from October 2020 through September 2022 for between $10,000 and $17,000.
Summary
CPSC recall: Ski-Doo snowmobiles. By Ski-Doo dealers nationwide from October 2020 through September 2022 for between $10,000 and $17,000.. Hazard: The fuel injector hose retainer screw can loosen and cause a fuel leak, posing a fire hazard.. Remedy: Consumers should immediately stop using the recalled snowmobiles and contact a Ski-Doo dealer to determine if their snowmobile is included in this recall and to schedule a free repair. BRP is contacting all known purchasers directly to coordinate the
Details
Source
CPSC Consumer Product Recall
External ID
9622
Action Date
2023-05-11
Status
Recalled
Category
consumer_product
Product Description
This recall involves Ski-Doo model years 2021 and 2022 snowmobiles equipped with 850 E-TEC and 850 E-TEC Turbo engines.
Company
Context & Analysis
This is a unclassified recall.
This was one of 13 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
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 (Ski-Doo dealers nationwide from October 2020 through September 2022 for between $10,000 and $17,000.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Ski-Doo dealers nationwide from October 2020 through September 2022 for between $10,000 and $17,000. have FDA actions?
This is the only FDA action we have on record for Ski-Doo dealers nationwide from October 2020 through September 2022 for between $10,000 and $17,000. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9622" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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