Model Year 2025-2026 CRF250R/RX/RWE and CRF450R/RX/RWE Off-Road Motorcycles
Summary
CPSC recall: Model Year 2025-2026 CRF250R/RX/RWE and CRF450R/RX/RWE Off-Road Motorcycles. By Authorized Honda Powersports dealers nationwide from June 2024 through March 2026 for between $8,900 and $13,200.. Hazard: The handlebar's clamp can unexpectedly cause the handlebar to rotate, posing a risk of serious injury or death due to a crash hazard.. Remedy: Consumers should stop using the recalled off-road motorcycles immediately and contact an authorized Honda Powersports dealer to schedule an a
Details
Source
CPSC Consumer Product Recall
External ID
10755
Action Date
2026-04-30
Status
Recalled
Category
consumer_product
Product Description
This recall involves model year 2025-2026 Honda off-road motorcycles with model numbers CRF250R/RX/RWE or CRF450R/RX/RWE
Context & Analysis
This is a unclassified recall.
This was one of 26 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 (Authorized Honda Powersports dealers nationwide from June 2024 through March 2026 for between $8,900 and $13,200.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Authorized Honda Powersports dealers nationwide from June 2024 through March 2026 for between $8,900 and $13,200. have FDA actions?
This is the only FDA action we have on record for Authorized Honda Powersports dealers nationwide from June 2024 through March 2026 for between $8,900 and $13,200. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "10755" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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