Proterra, Inc.
Summary
NHTSA campaign 22V114: Proterra, Inc. recalled for a safety defect. A loose steering gearbox can cause a loss of steering control, increasing the risk of a crash.
Details
Source
nhtsa
External ID
22V114
Action Date
2022-03-01
Status
Ongoing
Category
vehicle
Product Description
Proterra, Inc. (Proterra) is recalling certain 2017-2019 35 foot Catalyst E2, 2017-2019 40 foot E2, 2020-2021 35 foot RR, 2019-2020 40 foot RR, 2019-2022 40 foot ZX5, and 2020-2022 35 foot ZX5 buses. The plexus adhesive between the torque limiter plate and the bus body may be insufficient, causing the bolts that secure the steering gearbox to loosen.
Company
Context & Analysis
Proterra, Inc. has 2 FDA actions in our database.
Frequently Asked Questions
How often does Proterra, Inc. have FDA actions?
Proterra, Inc. has 2 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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