Lucid USA, Inc.
Summary
NHTSA campaign 26V017: Lucid USA, Inc. recalled for a safety defect. A rearview image that does not display reduces the driver's view behind the vehicle, increasing the risk of a crash.
Details
Source
nhtsa
External ID
26V017
Action Date
2026-01-20
Status
Ongoing
Category
vehicle
Product Description
Lucid USA, Inc. (Lucid) is recalling certain 2022-2026 Air vehicles equipped with an AD02 package and operating a software version from 2.8.0 through 2.8.16. The rearview camera image may not display when the vehicle is placed in reverse. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 111, "Rear Visibility."
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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