Volkswagen Group of America, Inc.
Summary
NHTSA campaign 22V901: Volkswagen Group of America, Inc. recalled for a safety defect. Missing weight information may result in unintentional overloading of the vehicle, increasing the risk of a crash.
Details
Source
nhtsa
External ID
22V901
Action Date
2022-12-08
Status
Ongoing
Category
vehicle
Product Description
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2023 Audi S3, RS3, and A3 vehicles. The Safety Certification label on the B-pillar is missing weight capacity information. As such, these vehicles fail to comply with the requirements of 49 CFR Part 567, "Certification."
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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