Volkswagen Group of America, Inc.
Summary
NHTSA campaign 22V102: Volkswagen Group of America, Inc. recalled for a safety defect. While referencing the B-pillar label, the operator may overload the vehicle, increasing the risk of a crash.
Details
Source
nhtsa
External ID
22V102
Action Date
2022-02-23
Status
Ongoing
Category
vehicle
Product Description
Volkswagen Group of America, Inc. (Audi) is recalling certain 2022 RS5 coupe and RS5 Sportback vehicles. The value for the maximum combined weight of occupants and cargo on the B-pillar Tire and Loading information label is incorrect. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 110, "Tire and Loading Information."
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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