RecallHawk

Agrish Adult Portable Bed Rails

Zhongshan Lebo Medical Co., Ltd., of China

Summary

CPSC recall: Agrish Adult Portable Bed Rails. By Zhongshan Lebo Medical Co., Ltd., of China. Hazard: The recalled bed rails violate the mandatory standard for adult portable bed rails because 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, posing a serious entrapment hazard and risk of death by asphyxiation.. Remedy: Consumers should immediately stop using the recalled adult portable bed rails and cont

Details

Source

CPSC Consumer Product Recall

External ID

10540

Action Date

2026-01-08

Status

Recalled

Category

consumer_product

Product Description

This recall involves Agrish-branded adult portable bed rails, models 2512, 2513, and 2516, for use on adult beds. The mo

Context & Analysis

This is a unclassified recall.

This was one of 16 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Zhongshan Lebo Medical 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 (Zhongshan Lebo Medical 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 Zhongshan Lebo Medical Co., Ltd., of China have FDA actions?

Zhongshan Lebo Medical 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 "10540" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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