Ferrari North America, Inc.
Summary
NHTSA campaign 26V152: Ferrari North America, Inc. recalled for a safety defect. Windows with insufficient light transmittance can impair the driver’s visibility, increasing the risk of a crash.
Details
Source
nhtsa
External ID
26V152
Action Date
2026-03-16
Status
Ongoing
Category
vehicle
Product Description
Ferrari North America, Inc. (Ferrari) is recalling certain 2025-2026 12Cilindri vehicles. The rear and side windows have less than 70% light transmittance which can obscure the driver's visibility. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 205, "Glazing Materials."
Company
Context & Analysis
Ferrari North America, Inc. has 8 FDA actions in our database.
Frequently Asked Questions
How often does Ferrari North America, Inc. have FDA actions?
Ferrari North America, Inc. has 8 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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