RecallHawk

Hearth & Hand™ with Magnolia Tea Kettles

Wazir Chand and Co Pvt Ltd, of Moradabad, India

Summary

CPSC recall: Hearth & Hand™ with Magnolia Tea Kettles. By Wazir Chand and Co Pvt Ltd, of Moradabad, India. Hazard: The paint can chip on the bottom of the recalled kettles, posing a fire hazard. In addition, the handle can break and/or the spout can leak, posing a risk of burn injuries.. Remedy: Consumers should immediately stop using the recalled tea kettles and return them to any Target store for a full refund or contact Target to receive a prepaid return label to return the tea kettle by mail

Details

Source

CPSC Consumer Product Recall

External ID

9413

Action Date

2022-10-06

Status

Recalled

Category

consumer_product

Product Description

This recall involves Hearth & Hand™ with Magnolia Tea Kettles. The 1.75 Quart (7 cup capacity) stainless steel tea kettl

Context & Analysis

This is a unclassified recall.

This was one of 14 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Wazir Chand and Co Pvt Ltd, of Moradabad, India 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 (Wazir Chand and Co Pvt Ltd, of Moradabad, India) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Wazir Chand and Co Pvt Ltd, of Moradabad, India have FDA actions?

Wazir Chand and Co Pvt Ltd, of Moradabad, India 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 "9413" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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