BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CADD LEGACY

    MDR report key: 1040312 · Received May 8, 2008

    Report

    Report Number
    MW5006763
    Event Type
    Injury
    Date Received
    May 8, 2008
    Date of Event
    February 7, 2008
    Report Date
    May 8, 2008
    Product Code
    FPA
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TN, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    DOES HAVE A CONCERN ABOUT SOME CASSETTES RECEIVED LATELY, AND RECEIVING A HI PRESSURE ALARM DURING PRIMING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CADD LEGACY CADD MEDICATION RESERVOIR FPA

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention