General Motors, LLC
Summary
NHTSA campaign 22E040: General Motors, LLC recalled for a safety defect. An inflator explosion may result in sharp metal fragments striking the driver or other occupants, resulting in serious i
Details
Source
nhtsa
External ID
22E040
Action Date
2022-05-19
Status
Ongoing
Category
vehicle
Product Description
General Motors, LLC (GM) is recalling certain Autoliv Front-Driver Air Bag Modules, with part numbers 20928235 and 20928242, sold as replacement parts for certain 2011-2012 GMC and Chevrolet vehicles. The driver's air bag inflator may explode during deployment, due to a manufacturing defect.
Company
Context & Analysis
General Motors, LLC has 163 FDA actions in our database.
Frequently Asked Questions
How often does General Motors, LLC have FDA actions?
General Motors, LLC has 163 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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