Volkswagen Group of America, Inc.
Summary
NHTSA campaign 22V064: Volkswagen Group of America, Inc. recalled for a safety defect. A rearview camera that does not display an image reduces the driver's rear view, increasing the risk of a crash.
Details
Source
nhtsa
External ID
22V064
Action Date
2022-02-08
Status
Ongoing
Category
vehicle
Product Description
Volkswagen Group of America, Inc. (Audi) is recalling certain 2022 Audi Q3 vehicles that failed to receive the software update under Recall 21V-825 (91CR). A software error may prevent the rearview image from initially displaying when the vehicle begins to reverse. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 111, "Rear Visibility."
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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