Hyundai Motor America
Summary
NHTSA campaign 21V938: Hyundai Motor America recalled for a safety defect. Inoperative headlights or taillights can decrease visibility for both the driver and surrounding traffic, increasing the
Details
Source
nhtsa
External ID
21V938
Action Date
2021-12-02
Status
Ongoing
Category
vehicle
Product Description
Hyundai Motor America (Hyundai) is recalling certain 2022 Tucson vehicles. The software installed in the Integrated Central Control Unit (ICU) may be incompatible with the vehicle, which could result in inoperative headlights and/or taillights.
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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