Subaru of America, Inc.
Summary
NHTSA campaign 23V080: Subaru of America, Inc. recalled for a safety defect. A 12-Volt battery that is unable to recharge can cause a loss of drive power, increasing the risk of a crash.
Details
Source
nhtsa
External ID
23V080
Action Date
2023-02-15
Status
Ongoing
Category
vehicle
Product Description
Subaru of America, Inc. (Subaru) is recalling certain 2019-2022 Crosstrek Hybrid vehicles. The harness terminal that supplies low-voltage power from the converter to the 12-Volt battery may corrode and break, preventing the 12-Volt battery from charging.
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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