RecallHawk

Easymake Adult Portable Bed Rails

Zhongshan Yungu Daily Products, of China

Summary

CPSC recall: Easymake Adult Portable Bed Rails. By Zhongshan Yungu Daily Products, of China. Hazard: The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required hazard warning labels.. Remedy: Consumers should stop using the recalled bed rails im

Details

Source

CPSC Consumer Product Recall

External ID

10696

Action Date

2026-04-09

Status

Recalled

Category

consumer_product

Product Description

This recall involves Easymake adult portable bed rails. The white and gray metal bed rails measure about 31.3 inches wid

Context & Analysis

This is a unclassified recall.

This was one of 30 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Zhongshan Yungu Daily Products, 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 (Zhongshan Yungu Daily Products, 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 Zhongshan Yungu Daily Products, of China have FDA actions?

Zhongshan Yungu Daily Products, 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 "10696" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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