Hyundai Motor America
Summary
NHTSA campaign 25V235: Hyundai Motor America recalled for a safety defect. Reduced braking performance and unexpected, continued acceleration increase the risk of a crash.
Details
Source
nhtsa
External ID
25V235
Action Date
2025-04-11
Status
Ongoing
Category
vehicle
Product Description
Hyundai Motor America (Hyundai) is recalling certain 2025 Hyundai IONIQ 5 "N" vehicles equipped with left-foot braking (LFB) and N e-shift features. The integrated electronic brake (IEB) and vehicle control unit (VCU) software may cause reduced braking performance when LFB is activated. Additionally, the vehicle may continue to accelerate after the pedal is released and the vehicle's N e-shift feature is engaged.
Company
Context & Analysis
Hyundai Motor America has 106 FDA actions in our database.
Frequently Asked Questions
How often does Hyundai Motor America have FDA actions?
Hyundai Motor America has 106 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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