Hyundai Motor America
Summary
NHTSA campaign 25V373: Hyundai Motor America recalled for a safety defect. Improperly aimed headlights can result in insufficient illumination of the road, decreasing the driver's visibility and
Details
Source
nhtsa
External ID
25V373
Action Date
2025-06-04
Status
Ongoing
Category
vehicle
Product Description
Hyundai Motor America (Hyundai) is recalling certain 2025 Hyundai IONIQ 5 vehicles. The right-side headlight may have an incorrect headlight aim label, which can result in improperly aimed headlights. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment."
Company
Context & Analysis
Hyundai Motor America has 106 FDA actions in our database.
Frequently Asked Questions
How often does Hyundai Motor America have FDA actions?
Hyundai Motor America has 106 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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