Volkswagen Group of America, Inc.
Summary
NHTSA campaign 22V224: Volkswagen Group of America, Inc. recalled for a safety defect. An incorrectly marked child restraint anchorage may cause confusion during child seat installation, resulting in a child
Details
Source
nhtsa
External ID
22V224
Action Date
2022-04-07
Status
Ongoing
Category
vehicle
Product Description
Volkswagen Group of America, Inc. (Audi) is recalling certain 2022 A3 Sedan and S3 Sedan vehicles. The child seat anchorage fitting sleeves are incorrectly marked with a different symbol than the one described in the owner's manual. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 225, "Child Restraint Anchorage Systems."
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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