Model Year 2026 Teryx4 H2 and Teryx5 H2 recreational off-road vehicles
Kawasaki Motors Manufacturing Corp., U.S.A., of Lincoln, Nebraska
Summary
CPSC recalled Model Year 2026 Teryx4 H2 and Teryx5 H2 recreational off-road vehicles by Kawasaki Motors Manufacturing Corp., U.S.A., of Lincoln, Nebraska. Hazard: The drive converter sheave can break in certain circumstances, resulting in metal fragments being discharged within the engine compartment and surrounding area, posing impact and injury hazards.. Remedy: Consumers should stop using the recalled vehicles immediately and contact a Kawasaki dealer to schedule a free repair. A technician will replace the moveable clutch sheave assembly, install a clutch cover guard and reprogram the Engine Control Unit (ECU) on the vehicle. Kawasaki is contacting all known purchasers directly..
Details
Source
cpsc
External ID
26550
Action Date
2026-06-11
Status
Ongoing
Category
product
Product Description
This recall involves Model Year 2026 Kawasaki Teryx4 H2 and Teryx5 H2 recreational off-road vehicles with the following model numbers: KRT1000D, KRT1000F and KRT1000G. Each unit has a unique VIN number located on the right rear of the main frame underneath the rear fender and above the rear wheel. The vehicles have either "Teryx4 H2" or "Teryx5 H2" on the driver and front passenger doors and the Kawasaki logo on both the left and right side above the rear wheels. The recalled vehicles were sold in lime green color. Model numbers are printed on the owner's manual.
Context & Analysis
Kawasaki Motors Manufacturing Corp., U.S.A., of Lincoln, Nebraska has 2 FDA actions in our database, including 1 recall.
Frequently Asked Questions
How often does Kawasaki Motors Manufacturing Corp., U.S.A., of Lincoln, Nebraska have FDA actions?
Kawasaki Motors Manufacturing Corp., U.S.A., of Lincoln, Nebraska has 2 FDA actions in our database, including 1 recall 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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