RYOBI Electric Pressure Washers
TTI Outdoor Power Equipment, Inc. (TTIOPE), of Anderson, South Carolina
Summary
CPSC recall: RYOBI Electric Pressure Washers. By TTI Outdoor Power Equipment, Inc. (TTIOPE), of Anderson, South Carolina. Hazard: The pressure washer's capacitor can overheat and burst, causing parts to be forcefully ejected, posing a risk of serious injury from impact to the user or bystanders.. Remedy: Consumers should immediately stop using the recalled pressure washers and visit https://www.ryobitools.com/recall to determine if their pressure washer is included in the recall and to receive a
Details
Source
CPSC Consumer Product Recall
External ID
10395
Action Date
2025-08-28
Status
Recalled
Category
consumer_product
Product Description
This recall involves Ryobi brushless electric pressure washers, models RY142300 and RY142711VNM. The recalled pressure w
Context & Analysis
This is a unclassified recall.
This was one of 8 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
TTI Outdoor Power Equipment, Inc. (TTIOPE), 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. (TTIOPE), 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. (TTIOPE), of Anderson, South Carolina have FDA actions?
TTI Outdoor Power Equipment, Inc. (TTIOPE), 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 "10395" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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