BEUDAMED
    FDA Adverse Event Other Summary report: N

    SARITA

    MDR report key: 324491 · Received April 6, 2001

    Report

    Report Number
    9617021-2001-00039
    Event Type
    Other
    Date Received
    April 6, 2001
    Date of Event
    January 25, 2001
    Report Date
    March 7, 2001
    Manufacturer
    ARJO, LTD.
    Product Code
    FSA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    THE FACILITY REPORTS THE HOIST HAD A FAULTY HANDSET. THE PT WAS UNABLE TO REMAIN SUPPORTED IN THE HOIST WHICH INDEPENDENTLY LOWERED THE PT TOWARDS THE FLOOR. TWO NURSES SUSTAINED BACK AND SHOULDER INJURIES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    15417 SARITA PATIENT LIFT FSA ARJO, LTD. KTBXXXX NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other