Volkswagen Group of America, Inc.
Summary
NHTSA campaign 22V178: Volkswagen Group of America, Inc. recalled for a safety defect. Worn bearings can cause the turbine wheel to contact the turbocharger housing or cause the shaft to break, causing an en
Details
Source
nhtsa
External ID
22V178
Action Date
2022-03-24
Status
Ongoing
Category
vehicle
Product Description
Volkswagen Group of America, Inc. (Audi) is recalling certain 2013-2017 A8, S6 Sedan, S7, S8, and 2014-2017 RS7 vehicles. The turbocharger oil supply strainer can become blocked, causing wear to the bearings due to lack of lubrication.
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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