Lucid USA, Inc.
Summary
NHTSA campaign 25E021: Lucid USA, Inc. recalled for a safety defect. Unintended acceleration increases the risk of a crash.
Details
Source
nhtsa
External ID
25E021
Action Date
2025-03-25
Status
Ongoing
Category
vehicle
Product Description
Lucid USA, Inc. (Lucid) is recalling certain All-Weather Floor Mats without anchors, model numbers ending in -00. Please see the recall report for a complete list of all affected part numbers. The floor mats may move and trap the accelerator pedal, causing unintended acceleration.
Company
Context & Analysis
Lucid USA, Inc. has 20 FDA actions in our database.
Frequently Asked Questions
How often does Lucid USA, Inc. have FDA actions?
Lucid USA, Inc. has 20 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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