BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MEDLINE

    MDR report key: 25195150 · Received May 16, 2026

    Report

    Report Number
    1417592-2026-01381
    Event Type
    Malfunction
    Date Received
    May 16, 2026
    Date of Event
    April 16, 2026
    Report Date
    May 16, 2026
    Manufacturer
    MEDLINE INDUSTRIES, LP
    Product Code
    LLI
    UDI-DI
    40080196320999
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    IT WAS REPORTED THAT THE WIRES ARE LOOS AND EXPOSED ON THE BED PENDANT AND THE FUNCTIONS NO LONGER WORK. THERE WERE NO REPORTS OF DEATH, SERIOUS INJURY, MEDICAL INTERVENTION, OR FOLLOW UP CARE. IT HAS BEEN DETERMINED THAT THE REPORTED EVENT COULD CAUSE OR CONTRIBUTE TO SERIOUS INJURY IF IT WERE TO OCCUR AGAIN. IN AN ABUNDANCE OF CAUTION, THIS IS A REPORTABLE EVENT. IF ADDITIONAL INFORMATION BECOMES AVAILABLE THIS REPORT WILL BE REOPENED AND REEVALUATED.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT THE WIRES ARE LOOS AND EXPOSED ON THE BED PENDANT AND THE FUNCTIONS NO LONGER WORK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    562341 MEDLINE BED,BASIC, SEMI ELECTRIC, 450 LB LLI MEDLINE INDUSTRIES, LP 40080196320999

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown