2024 CFORCE 800 Touring and 2024 CFORCE 1000 Touring All-Terrain Vehicles (ATVs)
Summary
CPSC recall: 2024 CFORCE 800 Touring and 2024 CFORCE 1000 Touring All-Terrain Vehicles (ATVs). By CFMOTO Powersports dealers nationwide from May 2024 through August 2024 for between $9,400 and $10,500.. Hazard: The throttle lever on the recalled ATVs can fail to return to the idle position when a driver releases it, and the vehicle could then unexpectedly continue to accelerate, posing a crash hazard.. Remedy: Consumers should immediately stop using the recalled ATVs and contact an authorized CF
Details
Source
CPSC Consumer Product Recall
External ID
10071
Action Date
2024-10-24
Status
Recalled
Category
consumer_product
Product Description
This recall involves 2024 CFORCE 800 Touring and 2024 CFORCE 1000 Touring ATVs. The recreational off highway vehicles we
Context & Analysis
This is a unclassified recall.
This was one of 7 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 (CFMOTO Powersports dealers nationwide from May 2024 through August 2024 for between $9,400 and $10,500.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does CFMOTO Powersports dealers nationwide from May 2024 through August 2024 for between $9,400 and $10,500. have FDA actions?
This is the only FDA action we have on record for CFMOTO Powersports dealers nationwide from May 2024 through August 2024 for between $9,400 and $10,500. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "10071" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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