BEUDAMED
    FDA Enforcement Class I Ongoing

    MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed, REF MDR107002E; 2) Semi Electric Basic Homecare Bed, 4-pack,REF MDR107002E-4

    Recall: Z-1011-2026 · Reported January 28, 2026

    Enforcement

    Recall Number
    Z-1011-2026
    Event ID
    98185
    Classification
    Class I
    Status
    Ongoing
    Product Type
    Devices
    Firm
    Medline Industries, LP
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    January 28, 2026
    Initiation Date
    November 26, 2025
    Classification Date
    January 16, 2026
    Address
    3 Lakes Dr, Northfield, IL, 60093-2753, United States

    Description

    MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed, REF MDR107002E; 2) Semi Electric Basic Homecare Bed, 4-pack,REF MDR107002E-4

    Reason

    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.

    Code Info

    1) UDI/DI 40080196320999, All lots; 2) UDI/DI 40080196320999, All Lots

    Distribution

    US, CA, PA, GUAM, VI

    Quantity

    373392 units