Lucid USA, Inc.
Summary
NHTSA campaign 24V836: Lucid USA, Inc. recalled for a safety defect. A loss of power to the rear drive unit can result in a complete loss of drive power, increasing the risk of a crash.
Details
Source
nhtsa
External ID
24V836
Action Date
2024-11-06
Status
Ongoing
Category
vehicle
Product Description
Lucid USA, Inc. (Lucid) is recalling certain 2024-2025 Air Pure rear wheel drive vehicles. The rear subframe wiring harness may be too short, straining the electrical connection and causing power loss to the rear drive unit (RDU).
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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