RecallHawk

Summary

CPSC recall: Fortemotus Adult Portable Bed Rails. By Guangzhou Kezhinuo Maoyi Youxian Gongsi, dba Fortemotus Direct US, 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. The bed rails do not meet structural stability or retention strap requirements, posing a fall hazard

Details

Source

CPSC Consumer Product Recall

External ID

10612

Action Date

2026-02-12

Status

Recalled

Category

consumer_product

Product Description

This recall involves Fortemotus-branded adult portable bed rails, model USFTMTJAS008. The recalled bed rails have black

Context & Analysis

This is a unclassified recall.

This was one of 26 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Guangzhou Kezhinuo Maoyi Youxian Gongsi, dba Fortemotus Direct US, 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 (Guangzhou Kezhinuo Maoyi Youxian Gongsi, dba Fortemotus Direct US, 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 Guangzhou Kezhinuo Maoyi Youxian Gongsi, dba Fortemotus Direct US, of China have FDA actions?

Guangzhou Kezhinuo Maoyi Youxian Gongsi, dba Fortemotus Direct US, 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 "10612" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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