Volkswagen Group of America, Inc.
Summary
NHTSA campaign 24V361: Volkswagen Group of America, Inc. recalled for a safety defect. Incorrect headlight control module software may cause the parking lights not to operate as intended when the headlights
Details
Source
nhtsa
External ID
24V361
Action Date
2024-05-23
Status
Ongoing
Category
vehicle
Product Description
Volkswagen Group of America, Inc. (Audi) is recalling certain 2022-2024 Q4 E-TRON and Q4 E-TRON Sportback vehicles. The incorrect headlight control module software may have been installed. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment."
Context & Analysis
Volkswagen Group of America, Inc. has 136 FDA actions in our database.
Frequently Asked Questions
How often does Volkswagen Group of America, Inc. have FDA actions?
Volkswagen Group of America, Inc. has 136 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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