DeWALT Battery Push walk-behind mowers and DeWALT Battery Self-Propelled walk-behind mowers
Summary
CPSC recall: DeWALT Battery Push walk-behind mowers and DeWALT Battery Self-Propelled walk-behind mowers. By Stanley Black and Decker Inc., of New Britain, Connecticut. Hazard: If water gets into the mower's handle support while the battery is installed, the mower can fail to shut off when the bail handle is released or start without a key, posing a laceration hazard to the user.. Remedy: Consumers should immediately stop using the recalled mowers if the mower has gotten wet and contact DeWALT t
Details
Source
CPSC Consumer Product Recall
External ID
10035
Action Date
2024-08-15
Status
Recalled
Category
consumer_product
Product Description
This recall involves 2024 model year DeWALT Battery 21" Push walk-behind mowers, model numbers DCMWP234U2 and DCMWP600X2
Context & Analysis
This is a unclassified recall.
This was one of 9 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Stanley Black and Decker Inc., of New Britain, Connecticut has 2 FDA actions in our database, including 1 recall.
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 (Stanley Black and Decker Inc., of New Britain, Connecticut) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Stanley Black and Decker Inc., of New Britain, Connecticut have FDA actions?
Stanley Black and Decker Inc., of New Britain, Connecticut has 2 FDA actions in our database, including 1 recall and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "10035" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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