Ducati North America
Summary
NHTSA campaign 25V838: Ducati North America recalled for a safety defect. Front or rear wheel lockup can cause a loss of motorcycle control, increasing the risk of a crash or injury.
Details
Source
nhtsa
External ID
25V838
Action Date
2025-12-08
Status
Ongoing
Category
vehicle
Product Description
Ducati North America (Ducati) is recalling certain 2025 Panigale V2 and 2025-2026 Ducati Streetfighter V2 motorcycles. The fuses for the ABS pump and control unit may have been reversed during assembly, which can cause an ABS malfunction and possibly result in wheel lockup.
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.
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