BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HP

    MDR report key: 214817 · Received March 10, 1999

    Report

    Report Number
    MW1015914
    Event Type
    Injury
    Date Received
    March 10, 1999
    Date of Event
    February 10, 1999
    Report Date
    March 9, 1999
    Manufacturer
    HEWLETT-PACKARD CO. MEDICAL PRODUCTS GROUP
    Product Code
    KLK
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    AZ, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    BLISTER NOTED AT PREVIOUSLY USED TCM SIGE AFTER PATCH WAS REMOVED ON THREE DAY OLD INFANT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HP HP TCP CO2/TCPO2 KLK HEWLETT-PACKARD CO. MEDICAL PRODUCTS GROUP * *

    Patients

    Seq Age Sex Outcome Treatment
    1 3 DAY Required Intervention