Volkswagen Group of America, Inc.
Summary
NHTSA campaign 25V233: Volkswagen Group of America, Inc. recalled for a safety defect. An incorrectly displayed warning light can fail to alert the driver to critical safety information, increasing the risk
Details
Source
nhtsa
External ID
25V233
Action Date
2025-04-11
Status
Ongoing
Category
vehicle
Product Description
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2025 ID. Buzz vehicles. The brake system warning light on the instrument panel display may be the incorrect symbol and color. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard numbers 135, "Light Vehicle Brake Systems" and 101, "Control and Displays."
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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