BRUTE FORCE® 750 All-Terrain Vehicles (ATVs)
Kawasaki Motors Manufacturing Corp. U.S.A., of Lincoln, Neb.
Summary
CPSC recall: BRUTE FORCE® 750 All-Terrain Vehicles (ATVs). By Kawasaki Motors Manufacturing Corp. U.S.A., of Lincoln, Neb.. Hazard: The fuel pump retainer plate bolts can come loose causing fuel leakage over time, posing a fire hazard.. Remedy: Consumers should immediately stop using the recalled vehicles and contact a Kawasaki dealer to schedule a free repair to replace the fuel pump retainer plate bolts. Kawasaki is contacting all known purchasers directly..
Details
Source
CPSC Consumer Product Recall
External ID
9045
Action Date
2021-04-22
Status
Recalled
Category
consumer_product
Product Description
This recall involves the 2021 BRUTE FORCE 750 4X4I EPS. The four-wheel all-terrain vehicles were sold in camo gray, brig
Context & Analysis
This is a unclassified recall.
This was one of 6 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, Neb. has 6 FDA actions in our database, including 3 recalls.
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, Neb.) 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, Neb. have FDA actions?
Kawasaki Motors Manufacturing Corp. U.S.A., of Lincoln, Neb. has 6 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9045" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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