Ducati North America
Summary
NHTSA campaign 23V377: Ducati North America recalled for a safety defect. Lights that automatically switch from low beams to the daylight position can reduce visibility during night riding, incr
Details
Source
nhtsa
External ID
23V377
Action Date
2023-05-30
Status
Ongoing
Category
vehicle
Product Description
Ducati North America (Ducati) is recalling certain 2020-2023 Panigale V2 motorcycles. The dashboard could automatically switch from low beam headlights to the headlight daylight position lamp (DRL), in automatic setting mode. As such, these motorcycles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment."
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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