Tow-Behind Field & Brush Mowers
Summary
CPSC recall: Tow-Behind Field & Brush Mowers. By DR Power Equipment, of South Burlington, Vermont, a subsidiary of Generac Power Systems Inc., of Waukesha, Wisconsin (through January 2018). Hazard: The exhaust pipe can break and cause damage to the unit due to excessive heat, especially in the presence of dry cuttings or spilled fuel, posing fire and burn hazards.. Remedy: Consumers should immediately stop using the recalled mowers and contact DR Power Equipment for a prorated refund or credit t
Details
Source
CPSC Consumer Product Recall
External ID
9752
Action Date
2023-11-09
Status
Recalled
Category
consumer_product
Product Description
This recall involves DR Power Equipment and Generac brand tow-behind field and brush mowers. The following model and ser
Context & Analysis
This is a unclassified recall.
This was one of 15 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 (through January 2018)) 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 (through January 2018) 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 (through January 2018) in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9752" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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