Dennis Eagle Inc.
Summary
NHTSA campaign 21V220: Dennis Eagle Inc. recalled for a safety defect. The incorrect illumination of the ABS warning light may cause the driver to believe the ABS has failed, changing driving
Details
Source
nhtsa
External ID
21V220
Action Date
2021-03-30
Status
Ongoing
Category
vehicle
Product Description
Dennis Eagle, Inc. (Dennis Eagle) is recalling certain 2017-2021 Elite and Proview vehicles. When the brake pads wear out, the ABS warning light may incorrectly illuminate in addition to the Brake Pad Wear warning light. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard numbers 101, "Control and Displays", and "Warning Devices."
Company
Context & Analysis
Dennis Eagle Inc. has 8 FDA actions in our database.
Frequently Asked Questions
How often does Dennis Eagle Inc. have FDA actions?
Dennis Eagle 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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