RecallHawk

FUFU&GAGA White Wood Frame Queen Size Murphy Wall Beds

Jiangsu Liangjiang Intelligent Furniture Co., Ltd, of China

Summary

CPSC recall: FUFU&GAGA White Wood Frame Queen Size Murphy Wall Beds. By Jiangsu Liangjiang Intelligent Furniture Co., Ltd, of China. Hazard: During assembly or disassembly, the 215-pound frame of the wall bed can fall onto consumers, posing deadly impact, crush, and laceration hazards.. Remedy: Consumers should immediately stop using the recalled wall beds and contact Ningbo Tianqi Electronic for a full refund. To obtain a refund, consumers will be provided with a disassembly kit that contains t

Details

Source

CPSC Consumer Product Recall

External ID

10508

Action Date

2025-12-04

Status

Recalled

Category

consumer_product

Product Description

This recall involves FUFU&GAGA white wood frame queen size Murphy wall beds. The beds are designed to be wall-mounted an

Context & Analysis

This is a unclassified recall.

This was one of 9 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Jiangsu Liangjiang Intelligent Furniture 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 Liangjiang Intelligent Furniture 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 Liangjiang Intelligent Furniture Co., Ltd, of China have FDA actions?

Jiangsu Liangjiang Intelligent Furniture 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 "10508" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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