RYOBI 40-Volt Brushless 21" Cordless Walk-Behind Mowers
TTI Outdoor Power Equipment Inc., of Anderson, South Carolina
Summary
CPSC recall: RYOBI 40-Volt Brushless 21" Cordless Walk-Behind Mowers. By TTI Outdoor Power Equipment Inc., of Anderson, South Carolina. Hazard: The recalled mowers have a push-on connector inside the powerhead that can overheat, posing a fire hazard.. Remedy: Consumers should immediately stop using the recalled mower and contact TTI Outdoor Power Equipment Inc. ("TTI") for instructions on how to disable the recalled mower and receive a free replacement 21" walk-behind mower..
Details
Source
CPSC Consumer Product Recall
External ID
10153
Action Date
2025-02-06
Status
Recalled
Category
consumer_product
Product Description
This recall involves certain RYOBI Brushless 21" Cordless Walk-Behind Self-Propelled Multi-Blade Push Mowers (40V HP). T
Context & Analysis
This is a unclassified recall.
This was one of 17 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
TTI Outdoor Power Equipment Inc., of Anderson, South Carolina 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 (TTI Outdoor Power Equipment Inc., of Anderson, South Carolina) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does TTI Outdoor Power Equipment Inc., of Anderson, South Carolina have FDA actions?
TTI Outdoor Power Equipment Inc., of Anderson, South Carolina 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 "10153" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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