RecallHawk

Honda Model EU7000is Portable Generators

American Honda Motor Co. Inc., of Torrance, California

Summary

CPSC recall: Honda Model EU7000is Portable Generators. By American Honda Motor Co. Inc., of Torrance, California. Hazard: The fuel filler cap can improperly seal, resulting in fuel and/or fuel vapor leaking, posing a fire hazard.. Remedy: Consumers should immediately stop using the recalled portable generators and contact an authorized Honda Power Equipment dealer to schedule an appointment for a free repair. Honda is contacting all known purchasers directly..

Details

Source

CPSC Consumer Product Recall

External ID

9677

Action Date

2023-08-03

Status

Recalled

Category

consumer_product

Product Description

This recall involves Honda Portable Generators with model number EU7000is. They are red and gray in color and measure ab

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.

American Honda Motor Co. Inc., of Torrance, California has 8 FDA actions in our database, including 4 recalls.

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 (American Honda Motor Co. Inc., of Torrance, California) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does American Honda Motor Co. Inc., of Torrance, California have FDA actions?

American Honda Motor Co. Inc., of Torrance, California has 8 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9677" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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