Model Year 2026 Teryx4 H2 and Teryx5 H2 recreational off-road vehicles
Kawasaki Motors Manufacturing Corp., U.S.A., of Lincoln, Nebraska
Summary
CPSC recall: 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 w
Details
Source
CPSC Consumer Product Recall
External ID
10814
Action Date
2026-06-11
Status
Recalled
Category
consumer_product
Product Description
This recall involves Model Year 2026 Kawasaki Teryx4 H2 and Teryx5 H2 recreational off-road vehicles with the following
Context & Analysis
This is a unclassified recall.
This was one of 25 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Kawasaki Motors Manufacturing Corp., U.S.A., of Lincoln, Nebraska has 2 FDA actions in our database, including 1 recall.
Frequently Asked Questions
What is a FDA recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Kawasaki Motors Manufacturing Corp., U.S.A., of Lincoln, Nebraska) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
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. Search for "10814" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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