RecallHawk

Summary

CPSC recall: Tow Behind Field and Brush Mowers. By DR Power Equipment, of South Burlington, Vermont, a subsidiary of Generac Power Systems Inc., of Waukesha, Wisconsin. Hazard: The blade carrier spindle bolt can become loose, causing the blade assembly to detach while the mower is in operation, posing a laceration hazard to the user.. Remedy: Consumers should immediately stop using the tow behind field and brush mower and contact DR Power to arrange for a free repair of the blade carrier assembl

Details

Source

CPSC Consumer Product Recall

External ID

10166

Action Date

2025-02-20

Status

Recalled

Category

consumer_product

Product Description

This recall involves DR Power Tow Behind Field and Brush Mowers. The black and orange tow behind mowers have the followi

Context & Analysis

This is a unclassified recall.

This was one of 23 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

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 (DR Power Equipment, of South Burlington, Vermont, a subsidiary of Generac Power Systems Inc., of Waukesha, Wisconsin) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does DR Power Equipment, of South Burlington, Vermont, a subsidiary of Generac Power Systems Inc., of Waukesha, Wisconsin have FDA actions?

This is the only FDA action we have on record for DR Power Equipment, of South Burlington, Vermont, a subsidiary of Generac Power Systems Inc., of Waukesha, Wisconsin in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "10166" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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