BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 296800 · Received September 15, 2000

    Report

    Report Number
    1035617-2000-00004
    Event Type
    Malfunction
    Date Received
    September 15, 2000
    Date of Event
    August 18, 2000
    Report Date
    August 25, 2000
    Manufacturer
    ZIMMER PATIENT CARE
    Product Code
    LFG
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MS, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    CAST CART TURNED OVER ON EMPLOYEE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * CAST CART LFG ZIMMER PATIENT CARE 3820 NI

    Patients

    Seq Age Sex Outcome Treatment
    1 27 YR Other