Thule, Inc.
Summary
NHTSA campaign 21E045: Thule, Inc. recalled for a safety defect. A detached rooftop tent may become a road hazard, increasing the risk of a crash.
Details
Source
nhtsa
External ID
21E045
Action Date
2021-05-13
Status
Ongoing
Category
vehicle
Product Description
Thule, Inc. (Thule) is recalling certain Thule Tepui Hybox Tepui Wedge part number 901110, Thule Tepui Hybox part number 901100, Tepui Hybox wedge part number 8001HB203, and Tepui Hybox part number 8001HB103 and 8001HB112 rooftop tents. The rooftop tent shell may crack at the point where the mounting rails attach and detach from the vehicle.
Company
Context & Analysis
Thule, Inc. has 2 FDA actions in our database.
Frequently Asked Questions
How often does Thule, Inc. have FDA actions?
Thule, Inc. has 2 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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