Volkswagen Group of America, Inc.
Summary
NHTSA campaign 21V413: Volkswagen Group of America, Inc. recalled for a safety defect. Adjusting the horizontal headlight beam can increase glare, reducing visibility for the driver and increasing the risk o
Details
Source
nhtsa
External ID
21V413
Action Date
2021-06-03
Status
Ongoing
Category
vehicle
Product Description
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2021 ID.4 vehicles. Caps were installed on the headlight vertical aim instead of the horizontal aim, allowing for horizontal adjustment of the headlight beam. 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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