Lucid USA, Inc.
Summary
NHTSA campaign 26V193: Lucid USA, Inc. recalled for a safety defect. A disconnected half shaft can result in a loss of drive power, increasing the risk of a crash.
Details
Source
nhtsa
External ID
26V193
Action Date
2026-03-27
Status
Ongoing
Category
vehicle
Product Description
Lucid USA, Inc. (Lucid) is recalling certain 2024-2026 Air vehicles equipped with Pure Rear-Wheel Drive. Improperly secured bolts may allow the half-shaft to disconnect from the drive unit.
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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