RecallHawk

Universal Broadmoore Cayden Gentleman's 9-drawer chests

Lacquer Craft Mfg. Co., Ltd of China, a subsidiary of Samson Holding Ltd.

Summary

CPSC recall: Universal Broadmoore Cayden Gentleman's 9-drawer chests. By Lacquer Craft Mfg. Co., Ltd of China, a subsidiary of Samson Holding Ltd.. Hazard: The recalled chests are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in death or serious injuries to consumers.. Remedy: Consumers should immediately stop using recalled chests if they are not properly anchored to the wall and place them in an area that children cannot access. Contact S

Details

Source

CPSC Consumer Product Recall

External ID

9348

Action Date

2022-07-07

Status

Recalled

Category

consumer_product

Product Description

This recall involves Samson International's Universal Broadmoore Cayden Gentleman's 9-drawer chests with model/item numb

Context & Analysis

This is a unclassified recall.

This was one of 10 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Lacquer Craft Mfg. Co., Ltd of China, a subsidiary of Samson Holding Ltd. 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 (Lacquer Craft Mfg. Co., Ltd of China, a subsidiary of Samson Holding Ltd.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Lacquer Craft Mfg. Co., Ltd of China, a subsidiary of Samson Holding Ltd. have FDA actions?

Lacquer Craft Mfg. Co., Ltd of China, a subsidiary of Samson Holding Ltd. 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 "9348" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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