RecallHawk

WeHwupe Adult Portable Bed Rails

Nanjing Chunqu Clothing Co. Ltd., of China

Summary

CPSC recall: WeHwupe Adult Portable Bed Rails. By Nanjing Chunqu Clothing Co. Ltd., of China. Hazard: The recalled bed rails violate federal regulations for adult portable bed rails, posing a serious entrapment hazard and risk of death by asphyxiation. When the bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress. In addition, the bed rails do not bear the required hazard warning labels.. Remedy: Consumers should sto

Details

Source

CPSC Consumer Product Recall

External ID

10284

Action Date

2025-05-29

Status

Recalled

Category

consumer_product

Product Description

This recall involves WeHwupe branded adult portable bed rails, models BRX-8002 and BRX-8003, sold for use on adult beds.

Context & Analysis

This is a unclassified recall.

This was one of 13 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Nanjing Chunqu Clothing 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 (Nanjing Chunqu Clothing 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 Nanjing Chunqu Clothing Co. Ltd., of China have FDA actions?

Nanjing Chunqu Clothing 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 "10284" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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