Honda Talon 1000 ROVs
American Honda Motor Co. Inc., of Timmonsville, South Carolina
Summary
CPSC recall: Honda Talon 1000 ROVs. By American Honda Motor Co. Inc., of Timmonsville, South Carolina. Hazard: The vehicle's intake funnel band screw can loosen and enter the engine through the intake funnel and cause sudden engine failure. If this occurs, it could result in a loss of control, increasing the risk of a crash or injury.. Remedy: Consumers should immediately stop using the recalled recreational off-highway vehicles and contact an authorized Honda Powersports dealer to schedule an a
Details
Source
CPSC Consumer Product Recall
External ID
9258
Action Date
2022-03-09
Status
Recalled
Category
consumer_product
Product Description
This recall involves model year 2019 - 2021 Honda Talon 1000 S2 and S4 recreational off-highway vehicles (ROVs). The veh
Context & Analysis
This is a unclassified recall.
This was one of 8 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
American Honda Motor Co. Inc., of Timmonsville, South Carolina has 2 FDA actions in our database, including 1 recall.
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 (American Honda Motor Co. Inc., of Timmonsville, South Carolina) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does American Honda Motor Co. Inc., of Timmonsville, South Carolina have FDA actions?
American Honda Motor Co. Inc., of Timmonsville, South Carolina has 2 FDA actions in our database, including 1 recall and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9258" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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