Porsche Cars North America, Inc.
Summary
NHTSA campaign 22V656: Porsche Cars North America, Inc. recalled for a safety defect. Improperly adjusted headlights may not illuminate the road properly, or cause a glare to oncoming drivers, which can inc
Details
Source
nhtsa
External ID
22V656
Action Date
2022-08-31
Status
Ongoing
Category
vehicle
Product Description
Porsche Cars North America, Inc. (Porsche) is recalling certain 2003-2020 Porsche Macan, Cayenne, Panamera, and Cayman S, 2001-2004 Boxster, Boxster S, 2004 Boxster 50 JAHRE SPYDER 550 vehicles. Please see the recall report for a complete list of all affected models and model years. The caps that cover the low-beam headlight horizontal adjustment screws are missing, which can allow the headlights to be improperly adjusted. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment."
Context & Analysis
Porsche Cars North America, Inc. has 49 FDA actions in our database.
Frequently Asked Questions
How often does Porsche Cars North America, Inc. have FDA actions?
Porsche Cars North America, Inc. has 49 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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