RecallHawk

Knob-control electric radiant cooktops, model GE JP3030

Haier US Appliance Solutions Inc., d/b/a GE Appliances, of Louisville, Kentucky

Summary

CPSC recall: Knob-control electric radiant cooktops, model GE JP3030. By Haier US Appliance Solutions Inc., d/b/a GE Appliances, of Louisville, Kentucky. Hazard: The cooktop's burners can remain on after use, even after being turned to the "off" position, due to misaligned burner knob stems and fractured burner knob components that can exist in units manufactured between July 2022 and September 2022, posing a burn hazard to consumers.. Remedy: Consumers should immediately contact GE Appliances t

Details

Source

CPSC Consumer Product Recall

External ID

9770

Action Date

2023-11-30

Status

Recalled

Category

consumer_product

Product Description

This recall involves GE-branded JP3030 knob-controlled electric radiant cooktops manufactured from July 2022 through Sep

Context & Analysis

This is a unclassified recall.

This was one of 11 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Haier US Appliance Solutions Inc., d/b/a GE Appliances, of Louisville, Kentucky 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 (Haier US Appliance Solutions Inc., d/b/a GE Appliances, of Louisville, Kentucky) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Haier US Appliance Solutions Inc., d/b/a GE Appliances, of Louisville, Kentucky have FDA actions?

Haier US Appliance Solutions Inc., d/b/a GE Appliances, of Louisville, Kentucky 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 "9770" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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