BMW of North America, LLC
Summary
NHTSA campaign 22V240: BMW of North America, LLC recalled for a safety defect. An air bag malfunction indicator light that fails to warn the driver of a problem increases the risk of injury in a cras
Details
Source
nhtsa
External ID
22V240
Action Date
2022-04-13
Status
Ongoing
Category
vehicle
Product Description
BMW of North America, LLC (BMW) is recalling certain 2022-2023 iX xDrive40, iX XDrive50, and iX M60 vehicles. The air bag malfunction indicator light and display message may not illuminate in the event of a problem with the air bag control or pedestrian protection systems, due to incorrect software.
Company
Context & Analysis
BMW of North America, LLC has 125 FDA actions in our database.
Frequently Asked Questions
How often does BMW of North America, LLC have FDA actions?
BMW of North America, LLC has 125 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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