BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ZIMMER

    MDR report key: 292997 · Received August 25, 2000

    Report

    Report Number
    MW1019807
    Event Type
    Malfunction
    Date Received
    August 25, 2000
    Date of Event
    August 18, 2000
    Report Date
    August 25, 2000
    Manufacturer
    ZIMMER, INC. PATIENT CARE DIV.
    Product Code
    LFG
    Product Problem
    Yes
    Report Source
    Voluntary 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 ZIMMER CAST CART LFG ZIMMER, INC. PATIENT CARE DIV. 3820 *

    Patients

    Seq Age Sex Outcome Treatment
    1 27 YR Other