MEDLINE beds labeled as: Semi Electric Lightweight Homecare Bed, REF MDR107002L
FDA Recall #Z-1012-2026 — Class I — November 26, 2025
Product Description
MEDLINE beds labeled as: Semi Electric Lightweight Homecare Bed, REF MDR107002L
Reason for Recall
Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as operating the bed above its specified weight limit, encountering an obstruction to bed movement, or experiencing jammed components/motor the hand pendant and pendant cords may overheat and, in rare instances, pose a risk of fire. Medline Industries, LP has received a total of (58) complaints associated with reports of pendant sparking, burning, melting, smoking or fire.
Recalling Firm
Medline Industries, LP — Northfield, IL
Classification
Class I — Reasonable probability of serious adverse health consequences or death.
Product Type
Devices
Product Quantity
13245 units
Distribution
US, CA, PA, GUAM, VI
Code Information
UDI/DI 40080196294320, All lots
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated