Sangohe Adult Portable Bed Rails
Summary
CPSC recalled Sangohe Adult Portable Bed Rails by Zhongshan KDB Health Solutions Co., Ltd., 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 warning labels.. Remedy: Consumers should immediately stop using the recalled adult portable bed rails and contact Sangohe for a full refund. Consumers should destroy the bed rails by cutting the handrails' foam padding and writing "RECALLED" on the upper and lower rails with permanent marker, take a photo of the destroyed rails and email the photo to SGHproductrecall@163.com..
Details
Source
cpsc
External ID
26378
Action Date
2026-04-02
Status
Ongoing
Category
product
Product Description
This recall involves Sangohe-branded adult portable bed rails models 504E and 504Q. Model 504E bed rail comes in black, measures 23 inches wide by 35 inches tall, and weighs nine pounds. The model number "504E" can be found on the outer packaging box, on the product label/sticker attached to the bed rail, and on the first page of the instruction manual. Model 504Q bed rail comes in black, measures 28.5 inches wide by 43.3 inches tall, and weighs nine pounds. The model number "504Q" can be found on the outer packaging box, on the product label/sticker attached to the bed rail, and on the first page of the instruction manual.
Context & Analysis
Zhongshan KDB Health Solutions Co., Ltd., of China has 2 FDA actions in our database, including 1 recall.
Frequently Asked Questions
How often does Zhongshan KDB Health Solutions Co., Ltd., of China have FDA actions?
Zhongshan KDB Health Solutions 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. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.
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