BEUDAMED
    FDA Recall Open, Classified

    MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed, REF MDR107003L

    Recall: Z-1015-2026 · Initiated November 26, 2025

    Recall

    Recall Number
    Z-1015-2026
    Event Number
    98185
    FEI Number
    1417592
    Product Code
    LLI
    Status
    Open, Classified
    Root Cause
    Device Design
    Initiated
    November 26, 2025
    Posted
    January 16, 2026
    Address
    3 Lakes Dr, Medline Industries, LP, Northfield, IL, 60093-2753

    Description

    MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed, REF MDR107003L

    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.

    Action

    Medline issued an URGENT MEDICAL DEVICE RECALL notice with an enclosed URGENT MEDICAL DEVICE FIELD CORRECTION NOTICE to its consignees on 11/26/2025 via email and USPS first class mail. The notice explained the issue, potential risks, and requested the user ONLY USE MEDLINE SIDE RAILS and MEDLINE ACCESSORIES that are intended for use with Medline Homecare Beds. When using Medline Side Rails and Medline Accessories, follow all applicable instructions for use. Distributors were directed to notify their customers. For questions, contact the Recall Department at 866-359-1704 [email protected].

    Distribution

    US, CA, PA, GUAM, VI

    Quantity

    35694 units