Navistar, Inc.
Summary
NHTSA campaign 21V227: Navistar, Inc. recalled for a safety defect. Unintended spring brake application may occur, increasing the risk of a crash.
Details
Source
nhtsa
External ID
21V227
Action Date
2021-04-01
Status
Ongoing
Category
vehicle
Product Description
Navistar, Inc. (Navistar) is recalling certain 2021 International LT, RH, MV, and HV vehicles equipped with Bendix pressure switches. A retainer was not properly seated in the SC-3 single check valve and may not provide source air isolation when pressure is applied. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 121, "Air Brake Systems."
Company
Context & Analysis
Navistar, Inc. has 58 FDA actions in our database.
Frequently Asked Questions
How often does Navistar, Inc. have FDA actions?
Navistar, Inc. has 58 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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