BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EASYCARE BED

    MDR report key: 25099030 · Received May 6, 2026

    Report

    Report Number
    3009402404-2026-00010
    Event Type
    Malfunction
    Date Received
    May 6, 2026
    Date of Event
    April 1, 2026
    Report Date
    May 6, 2026
    Manufacturer
    JOERNS HEALTHCARE
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SC, US
    Reporter Occupation
    501

    Narratives

    Additional Manufacturer Narrative · 0

    THIS REPORT OR OTHER INFORMATION SUBMITTED BY JOERNS HEALTHCARE UNDER 21 CFR PART 803, AND RELEASE BY FDA OF THAT REPORT INFORMATION, DOES NOT REFLECT A CONCLUSION OR ADMISSION BY JOERNS HEALTHCARE, ITS EMPLOYEES, ITS CONTRACT SERVICE FIRMS, OR THEIR EMPLOYEES, FINISHED DEVICE SUPPLIERS, OR THEIR EMPLOYEES CAUSED OR CONTRIBUTED TO THE REPORTABLE EVENT.

    Description of Event or Problem · 0

    IT WAS REPORTED TO THE MANUFACTURER BY THE END USER: A RESIDENT HAD JUST ADMITTED TO THE FACILITY, AND WITHIN 20 MINUTES OF BEING PLACED IN THE BED, IT COLLAPSED. FORTUNATELY, THERE DID NOT APPEAR TO BE ANY HARM TO THE RESIDENT. UPON INSPECTION, THE DRIVE ARM HAD BROKEN THROUGH THE MOTOR CASING CAUSING IT TO COLLAPSE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    156493 EASYCARE BED PATIENT BED FNL JOERNS HEALTHCARE ECSBED

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Male