Volkswagen Group of America, Inc.
Summary
NHTSA campaign 21V198: Volkswagen Group of America, Inc. recalled for a safety defect. A deactivated passenger air bag increases the risk of injury during a crash.
Details
Source
nhtsa
External ID
21V198
Action Date
2021-03-23
Status
Ongoing
Category
vehicle
Product Description
Volkswagen Group of America, Inc. (Audi) is recalling certain 2015-2020 Audi S3 Sedan, A3 Sedan, 2016-2018 A3 Etron, 2017-2020 RS3 Sedan, and 2015-2019 A3 Cabriolet vehicles. The passenger occupant detection system (PODS) may malfunction and switch off the passenger air bag even when the seat is occupied.
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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