Lippert
Summary
NHTSA campaign 23E050: Lippert recalled for a safety defect. An axle that moves out of position can cause a loss of vehicle control and increase the risk of a crash.
Details
Source
nhtsa
External ID
23E050
Action Date
2023-07-06
Status
Ongoing
Category
vehicle
Product Description
Lippert (Lippert) is recalling certain Curt 7000 and 8000 lb axles. The U-bolts may have been improperly tightened, which can cause the axle to move out of position.
Company
Context & Analysis
Lippert has 17 FDA actions in our database.
Frequently Asked Questions
How often does Lippert have FDA actions?
Lippert has 17 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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