Subaru of America, Inc.
Summary
NHTSA campaign 22V838: Subaru of America, Inc. recalled for a safety defect. The seat belt assembly may not properly restrain an occupant during a crash, increasing the risk of injury.
Details
Source
nhtsa
External ID
22V838
Action Date
2022-11-14
Status
Ongoing
Category
vehicle
Product Description
Subaru of America, Inc. (Subaru) is recalling certain 2009-2013 Forester vehicles. The front seat belt assembly force-limiter may not operate correctly in the event of a crash.
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.
Want to know the moment something like this happens?
Get alerts for vehicle