Subaru of America, Inc.
Summary
NHTSA campaign 22V624: Subaru of America, Inc. recalled for a safety defect. Reflectors that do not provide adequate illumination reduce the driver's ability to see and increase the risk of a crash
Details
Source
nhtsa
External ID
22V624
Action Date
2022-08-12
Status
Ongoing
Category
vehicle
Product Description
Subaru of America, Inc. (Subaru) is recalling certain 2017-2019 Impreza vehicles. The left and right side reflex reflector and left side low beam reflector may inadequately reflect light. 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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