Mobility Source Medical Technology Co., Ltd, of China recalls

2 recalls recorded since 2018, most recently on 30 April 2026. Status and classification are as published by the CPSC.

Recalls2

Ongoing (FDA)0

Terminated or completed0

Class I (FDA)0

Recall started: 30 April 2026
Reason: 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.
Recall number: 26449

Recall started: 23 October 2025
Reason: 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.
Recall number: 26037

A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.