RecallHawk

Romorgniz Fabric 12- and 13-Drawer Dressers

Baituo Innovation Technology Co. Ltd., dba Romorgniz, of China

Summary

CPSC recalled 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 them in an area that children cannot access. Contact Romorgniz for instructions on how to dispose of the dressers to receive a full refund. Consumers must submit a photo to Romorgnizrecall@outlook.com demonstrating disposal of the product..

Details

Source

cpsc

External ID

26106

Action Date

2025-11-20

Status

Ongoing

Category

product

Product Description

This recall involves Romorgniz Fabric 12- and 13-Drawer Dressers. The dressers come in rustic brown, black, pink and white and have a metal frame and wooden top. The 12-drawer dresser has 12 collapsable fabric drawers, and the 13-drawer dresser has 13 collapsable fabric drawers. The 12-drawer dressers measure about 52 inches by 12 inches by 35 inches. The 13-drawer dressers measure about 35 inches by 11 inches by 55 inches. The 12-drawer dressers have "Model No.: R99MWM12CHMW" printed on the back and the 13-drawer dressers have "Model No.: R99M9C4CLHW" printed on the back.

Context & Analysis

Baituo Innovation Technology Co. Ltd., dba Romorgniz, of China has 2 FDA actions in our database, including 1 recall.

Frequently Asked Questions

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. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.

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