BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FULL ELECTRIC HILO BED

    MDR report key: 24381398 · Received February 18, 2026

    Report

    Report Number
    3009402404-2026-00003
    Event Type
    Malfunction
    Date Received
    February 18, 2026
    Date of Event
    January 26, 2026
    Report Date
    February 18, 2026
    Manufacturer
    JOERNS HEALTHCARE
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    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: THE BED BROKE OFF FROM THE WELDED PARTS AS THE STAFF WERE LIFTING THE BED TO PERFORM PATIENT CARE. PATIENT WAS IN BED. PATIENT WAS NOT INJURED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    195715 FULL ELECTRIC HILO BED FULL ELEC HILO BED FNL JOERNS HEALTHCARE PAN1000-FLEX-RAH

    Patients

    Seq Age Sex Outcome Treatment
    1 65 YR Male