Kia America, Inc.
Summary
NHTSA campaign 23V649: Kia America, Inc. recalled for a safety defect. Front lower control arm failure can cause a sudden loss of steering control, increasing the risk of a crash.
Details
Source
nhtsa
External ID
23V649
Action Date
2023-09-22
Status
Ongoing
Category
vehicle
Product Description
Kia America, Inc. (Kia) is recalling certain 2023 Forte vehicles. The right front lower control arm may have been improperly welded, which can cause it to fail.
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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