LEACHOI Bed Rail
Summary
CPSC recalled LEACHOI Bed Rail by Mobility Source Medical Technology 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. In addition, the bed rails do not bear the required hazard warning labels.. Remedy: Consumers should stop using the recalled adult portable bed rails immediately and contact LEACHOI Store to obtain a refund. Consumers should follow these disposal steps: 1 Remove the bed rail handle, U-shaped frame, side handle, and extension tubes (if present). 2 Write "RECALLED" on upper rail handle and silver U-shaped frame with a permanent marker. 3 Using scissors, cut the black fabric mesh bag off the upper rail and cut the black safety strap in half (if present). 4 Write the buyer's name on a piece of paper next to the disassembled product. 5 Take a photo and upload it online at https://leachoi.com/leachoi-bed-rail-safety-recall/. 6 Dispose of the recalled product in accordance with local requirements. Consumers who have difficulty with any disposal step or need additional instruction should contact LEACHOI Store..
Details
Source
cpsc
External ID
26037
Action Date
2025-10-23
Status
Ongoing
Category
product
Product Description
This recall involves LEACHOI Bed Rails, ASIN B0BZVCG2R5. The bed rail comes in black/silver and weighs 7.72 pounds. The product measures 15.6 inches by 25.4 inches by 24 inches.
Context & Analysis
Mobility Source Medical Technology Co., Ltd, of China has 4 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
How often does Mobility Source Medical Technology Co., Ltd, of China have FDA actions?
Mobility Source Medical Technology Co., Ltd, of China has 4 FDA actions in our database, including 2 recalls 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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