Thule, Inc.
Summary
NHTSA campaign 22E091: Thule, Inc. recalled for a safety defect. A detached bike arm assembly can fall into the roadway, increasing the risk of a crash.
Details
Source
nhtsa
External ID
22E091
Action Date
2022-10-24
Status
Ongoing
Category
vehicle
Product Description
Thule, Inc. (Thule) is recalling certain Thule Range, Camber 2, and Camber 4 bike carriers. The weld on the on the bike arm assembly may be defective, causing the bike arm assembly to detach.
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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