Northern Tool & Equipment Powerhorse 13000ES Portable Generators
Summary
CPSC recall: Northern Tool & Equipment Powerhorse 13000ES Portable Generators. By Northern Tool & Equipment stores nationwide and online at www.northerntool.com from July 2016 through September 2020 for about $1,850.. Hazard: The portable generators have a wiring error which can result in an electrical shock to users.. Remedy: Consumers should immediately stop using the recalled generators and contact Northern Tool & Equipment to schedule a free repair by an authorized dealer..
Details
Source
CPSC Consumer Product Recall
External ID
9004
Action Date
2021-02-24
Status
Recalled
Category
consumer_product
Product Description
This recall involves Northern Tool & Equipment Powerhorse 13000ES Portable Generator Model #799215. The gasoline generat
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.
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 (Northern Tool & Equipment stores nationwide and online at www.northerntool.com from July 2016 through September 2020 for about $1,850.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Northern Tool & Equipment stores nationwide and online at www.northerntool.com from July 2016 through September 2020 for about $1,850. have FDA actions?
This is the only FDA action we have on record for Northern Tool & Equipment stores nationwide and online at www.northerntool.com from July 2016 through September 2020 for about $1,850. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9004" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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