RecallHawk

Bobcat-branded and Kubota-branded stand-on zero-turn lawnmowers

Doosan Bobcat North America, of West Fargo, North Dakota

Summary

CPSC recall: Bobcat-branded and Kubota-branded stand-on zero-turn lawnmowers. By Doosan Bobcat North America, of West Fargo, North Dakota. Hazard: The dampers installed on the steering system of the mower can prevent the control levers from returning to the neutral position and the Operator Presence switch will not activate and stop the engine and blades, posing crash and laceration hazards to the operator or bystanders.. Remedy: Consumers should immediately stop using the recalled lawnmowers an

Details

Source

CPSC Consumer Product Recall

External ID

9744

Action Date

2023-10-26

Status

Recalled

Category

consumer_product

Product Description

This recall involves Bobcat-branded and Kubota-branded stand-on zero-turn lawnmowers. The Bobcat stand-on zero-turn lawn

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.

Doosan Bobcat North America, of West Fargo, North Dakota 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 (Doosan Bobcat North America, of West Fargo, North Dakota) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Doosan Bobcat North America, of West Fargo, North Dakota have FDA actions?

Doosan Bobcat North America, of West Fargo, North Dakota 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 "9744" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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