Ducati North America
Summary
NHTSA campaign 23V250: Ducati North America recalled for a safety defect. A broken foot peg can cause the passenger to suddenly lose their foot support, increasing the risk of crash or injury.
Details
Source
nhtsa
External ID
23V250
Action Date
2023-04-07
Status
Ongoing
Category
vehicle
Product Description
Ducati North America (Ducati) is recalling certain 2023 Diavel V4 motorcycles. The right and/or left side passenger foot pegs may break while mounting or riding the motorcycle.
Company
Context & Analysis
Ducati North America has 10 FDA actions in our database.
Frequently Asked Questions
How often does Ducati North America have FDA actions?
Ducati North America has 10 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.
Want to know the moment something like this happens?
Get alerts for vehicle