Roadtrek Inc.
Summary
NHTSA campaign 26V271: Roadtrek Inc. recalled for a safety defect. A pop-top that lifts during transit can distract the driver, or detach if the secondary safety straps fail, increasing t
Details
Source
nhtsa
External ID
26V271
Action Date
2026-04-29
Status
Ongoing
Category
vehicle
Product Description
Roadtrek Inc. (Roadtrek) is recalling certain 2024-2026 Westfalia Wave SL, 2022-2026 Zion Slumber, Play Slumber, 2026 Play Tuff SL, 2025-2026 Play+Slumber, and 2024 Pivot Slumber recreational vehicles. The pop-top latch may disengage during transit, causing the pop-top to lift.
Company
Context & Analysis
Roadtrek Inc. has 11 FDA actions in our database.
Frequently Asked Questions
How often does Roadtrek Inc. have FDA actions?
Roadtrek Inc. has 11 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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