Hepo Adult Portable Bed Rails
Summary
CPSC recalled Hepo Adult Portable Bed Rails by Mobility Source Medical Technology 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. The bed rails also do not meet structural stability or retention strap requirements, posing a fall hazard. The bed rails' push pins and push pin holes are incorrectly sized, posing a laceration hazard. 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 Hepo Care Medical Equipment Online for a full refund. Consumers will be asked to destroy the bed rails by dismantling the bed rails, cutting off the storage bag and writing "RECALLED" on the upper and lower rails with permanent marker, take a photo of the destroyed rails and upload the photo to www.hepolife.com/bed-rail-safety-recall or email the photo to manager@lqxmedical.com..
Details
Source
cpsc
External ID
26449
Action Date
2026-04-30
Status
Ongoing
Category
product
Product Description
This recall involves Hepo-branded adult portable bed rails, model 110039. The recalled bed rails have white tubing with black foam rubber handle grips, a black fabric pouch, and measures about 16 inches wide by 25 inches high. The model number is located on the original product packaging.
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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