BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HOYER HPL700WSC-S2

    MDR report key: 24416258 · Received February 23, 2026

    Report

    Report Number
    3009402404-2026-00005
    Event Type
    Malfunction
    Date Received
    February 23, 2026
    Date of Event
    January 28, 2026
    Report Date
    February 23, 2026
    Manufacturer
    JOERNS HEALTHCARE
    Product Code
    FSA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN, 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: CUSTOMER HAS THIS LIFT AND IS USING HOYER SLING NA25711. THEY SAID A RESIDENT FELL BECAUSE SHE WAS MOVING IN THE SLING AND SHIFTED TO ONE SIDE, AND IT MADE THE LOOP COME OFF OF THE CRADLE AND SHE FELL OUT!

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    478918 HOYER HPL700WSC-S2 PATIENT LIFT FSA JOERNS HEALTHCARE HLP700WSC-S2

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Female