Romorgniz Fabric 12- and 13-Drawer Dressers
Baituo Innovation Technology Co. Ltd., dba Romorgniz, of China
Summary
CPSC recall: Romorgniz Fabric 12- and 13-Drawer Dressers. By Baituo Innovation Technology Co. Ltd., dba Romorgniz, 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 th
Details
Source
CPSC Consumer Product Recall
External ID
10495
Action Date
2025-11-20
Status
Recalled
Category
consumer_product
Product Description
This recall involves Romorgniz Fabric 12- and 13-Drawer Dressers. The dressers come in rustic brown, black, pink and whi
Context & Analysis
This is a unclassified recall.
This was one of 16 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Baituo Innovation Technology Co. Ltd., dba Romorgniz, 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 (Baituo Innovation Technology Co. Ltd., dba Romorgniz, 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 Baituo Innovation Technology Co. Ltd., dba Romorgniz, of China have FDA actions?
Baituo Innovation Technology Co. Ltd., dba Romorgniz, 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 "10495" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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