Kia America, Inc.
Summary
NHTSA campaign 23V692: Kia America, Inc. recalled for a safety defect. A headliner plate that detaches during a crash may strike an occupant, increasing their risk of injury.
Details
Source
nhtsa
External ID
23V692
Action Date
2023-10-16
Status
Ongoing
Category
vehicle
Product Description
Kia America, Inc. (Kia) is recalling certain 2009-2014 Borrego vehicles. The headliner plates may not be secured properly, which can result in the plates detaching in the event of a side curtain air bag deployment.
Company
Context & Analysis
Kia America, Inc. has 70 FDA actions in our database.
Frequently Asked Questions
How often does Kia America, Inc. have FDA actions?
Kia America, Inc. has 70 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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