Subaru of America, Inc.
Summary
NHTSA campaign 23V016: Subaru of America, Inc. recalled for a safety defect. Incorrect instructions for adjusting the sensitivity of the High Beam Assist function contained in the owner's manual ma
Details
Source
nhtsa
External ID
23V016
Action Date
2023-01-23
Status
Ongoing
Category
vehicle
Product Description
Subaru of America, Inc. (Subaru) is recalling certain 2022 WRX vehicles equipped with the "Eyesight" feature. The owner's manual may contain incorrect instructions for adjusting the sensitivity of the High Beam Assist function. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment."
Company
Context & Analysis
Subaru of America, Inc. has 28 FDA actions in our database.
Frequently Asked Questions
How often does Subaru of America, Inc. have FDA actions?
Subaru of America, Inc. has 28 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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