RecallHawk

17 Stories Furniture 18-Drawer Dressers

Jiangsu Quanronghe Smart Home Co., Ltd., of China

Summary

CPSC recall: 17 Stories Furniture 18-Drawer Dressers. By Jiangsu Quanronghe Smart Home Co., Ltd., of China. Hazard: The recalled dressers are unstable if they are not anchored to the wall, posing serious tip-over and entrapment hazard that can result in injuries or death to children. The dressers violate the mandatory standard as required by the STURDY Act.. Remedy: Consumers should stop using the recalled dressers immediately if they are not anchored to the wall and place them in an area that c

Details

Source

CPSC Consumer Product Recall

External ID

10531

Action Date

2025-12-18

Status

Recalled

Category

consumer_product

Product Description

This recall involves 17 Stories Furniture 18-Drawer Dressers. The recalled dressers were sold in black, brown and gray.

Context & Analysis

This is a unclassified recall.

This was one of 23 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Jiangsu Quanronghe Smart Home Co., Ltd., of China 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 (Jiangsu Quanronghe Smart Home Co., Ltd., of China) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Jiangsu Quanronghe Smart Home Co., Ltd., of China have FDA actions?

Jiangsu Quanronghe Smart Home Co., Ltd., of China 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 "10531" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for consumer_product

Related Actions