RecallHawk

Kawasaki Lawn Mower Engines used in Ariens, Gravely, Husqvarna, John Deere and RedMax brand lawn mowers

Kawasaki Motors Manufacturing Corp. U.S.A., of Maryville, Missouri

Summary

CPSC recall: Kawasaki Lawn Mower Engines used in Ariens, Gravely, Husqvarna, John Deere and RedMax brand lawn mowers. By Kawasaki Motors Manufacturing Corp. U.S.A., of Maryville, Missouri. Hazard: The fuel tube could have been damaged due to improper workmanship while removing the fuel tube for repair, which could cause a fuel leak, posing fire and burn hazards.. Remedy: Consumers should immediately stop using the recalled engines used in lawn and garden equipment and contact Kawasaki Motors Man

Details

Source

CPSC Consumer Product Recall

External ID

9743

Action Date

2023-10-26

Status

Recalled

Category

consumer_product

Product Description

This recall involves Kawasaki engines used in riding lawn mowers sold under the Ariens brand name with mower models IKON

Context & Analysis

This is a unclassified recall.

This was one of 7 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 Maryville, Missouri has 4 FDA actions in our database, including 2 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 Maryville, Missouri) 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 Maryville, Missouri have FDA actions?

Kawasaki Motors Manufacturing Corp. U.S.A., of Maryville, Missouri has 4 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9743" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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