BEUDAMED
    FDA Adverse Event Death Summary report: N

    HOYER SLING

    MDR report key: 275634 · Received April 28, 2000

    Report

    Report Number
    2182598-2000-00013
    Event Type
    Death
    Date Received
    April 28, 2000
    Date of Event
    April 6, 2000
    Manufacturer
    SUNRISE MEDICAL INC. / PCP HOYER DIVISION
    Product Code
    FSA
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE RESIDENT WAS BEING TRANSFERRED WHEN IT WAS ALLEGED THAT THE SLING RIPPED CAUSING THE RESIDENT TO FALL TO THE FLOOR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HOYER SLING PATIENT LIFTER ACCESSORY FSA SUNRISE MEDICAL INC. / PCP HOYER DIVISION 112-C NA

    Patients

    Seq Age Sex Outcome Treatment
    1 87 YR Death