Lucid USA, Inc.
Summary
NHTSA campaign 26V192: Lucid USA, Inc. recalled for a safety defect. Seat bracket failure can increase the risk of injury during a crash.
Details
Source
nhtsa
External ID
26V192
Action Date
2026-03-27
Status
Ongoing
Category
vehicle
Product Description
Lucid USA, Inc. (Lucid) is recalling certain 2025-2026 Gravity vehicles. The lap belt anchor brackets on the second row seats may have insufficient welds, which can cause bracket failure. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard numbers 207, “Seating Systems” and 210, “Seat Belt Assembly Anchorages.”
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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