RecallHawk

Summary

CPSC recall: KKL Fabric 9-Drawer Dressers. By Changzhou Municipal Sea Metal Products Co. Ltd., of China. Hazard: The recalled dressers are unstable if they are not anchored to the wall, posing a serious tip-over and entrapment hazards 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

10534

Action Date

2025-12-18

Status

Recalled

Category

consumer_product

Product Description

This recall involves KKL Fabric 9-Drawer Dressers. The recalled dressers were sold in black, brown and white. They have

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.

Changzhou Municipal Sea Metal Products Co. Ltd., of China has 4 FDA actions in our database, including 2 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 (Changzhou Municipal Sea Metal Products 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 Changzhou Municipal Sea Metal Products Co. Ltd., of China have FDA actions?

Changzhou Municipal Sea Metal Products Co. Ltd., of China has 4 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "10534" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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