Subaru of America, Inc.
Summary
NHTSA campaign 26V436: Subaru of America, Inc. recalled for a safety defect. An incorrect GAWR label may lead to an overloaded vehicle, increasing the risk of a crash.
Details
Source
nhtsa
External ID
26V436
Action Date
2026-07-08
Status
Ongoing
Category
vehicle
Product Description
Subaru of America, Inc. (Subaru) is recalling certain 2026 Crosstrek Hybrid, 2025-2026 Forester Hybrid, Forester, and 2019-2026 Ascent vehicles. These vehicles were manufactured with an incorrect Gross Axle Weight Rating (GAWR) on the certification label. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) 110, "Tire selection and rims."
Company
Context & Analysis
Subaru of America, Inc. has 28 FDA actions in our database.
Frequently Asked Questions
How often does Subaru of America, Inc. have FDA actions?
Subaru of America, Inc. has 28 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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