WLIVE Fabric 16-Drawer Dressers
Summary
CPSC recall: WLIVE Fabric 16-Drawer Dressers. By Jiangsu Zhi Pai Furniture Manufacturing Co., Ltd., of China. Hazard: The recalled dressers are unstable if they are not anchored to the wall, posing 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 t
Details
Source
CPSC Consumer Product Recall
External ID
10466
Action Date
2025-10-30
Status
Recalled
Category
consumer_product
Product Description
This recall expansion involves WLIVE Fabric 16-drawer dressers. The recalled dressers were sold in charcoal black, charc
Context & Analysis
This is a unclassified recall.
This was one of 25 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Jiangsu Zhi Pai Furniture Manufacturing 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 (Jiangsu Zhi Pai Furniture Manufacturing 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 Zhi Pai Furniture Manufacturing Co., Ltd., of China have FDA actions?
Jiangsu Zhi Pai Furniture Manufacturing 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 "10466" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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