Maserati North America, Inc.
Summary
NHTSA campaign 25V722: Maserati North America, Inc. recalled for a safety defect. Improperly aimed headlights can result in insufficient illumination of the road, reducing the driver's visibility, and i
Details
Source
nhtsa
External ID
25V722
Action Date
2025-10-24
Status
Ongoing
Category
vehicle
Product Description
Maserati North America, Inc. (Maserati) is recalling certain 2024-2025 Grancabrio, 2024-2025 Granturismo, and 2023-2025 Grecale vehicles. The headlights may be missing adjustment prevention caps, which can allow the headlights to be improperly adjusted. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamp, Reflective Devices and Associated Equipment."
Company
Context & Analysis
Maserati North America, Inc. has 10 FDA actions in our database.
Frequently Asked Questions
How often does Maserati North America, Inc. have FDA actions?
Maserati North America, Inc. 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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