Piaggio Group Americas, Inc.
Summary
NHTSA campaign 22V217: Piaggio Group Americas, Inc. recalled for a safety defect. Brakes that do not perform as expected, and require the driver to apply more force to the brake levers or pedals, increa
Details
Source
nhtsa
External ID
22V217
Action Date
2022-04-04
Status
Ongoing
Category
vehicle
Product Description
Piaggio Group Americas, Inc. (Piaggio) is recalling certain 2020-2021 MP3 500 HPE scooters. The brake hose terminal fittings zinc plating may contaminate the brake fluid, decreasing brake performance.
Company
Context & Analysis
Piaggio Group Americas, Inc. has 4 FDA actions in our database.
Frequently Asked Questions
How often does Piaggio Group Americas, Inc. have FDA actions?
Piaggio Group Americas, Inc. has 4 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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