BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 1031971 · Received April 4, 2008

    Report

    Report Number
    1031971
    Event Type
    Malfunction
    Date Received
    April 4, 2008
    Date of Event
    March 26, 2008
    Report Date
    April 4, 2008
    Manufacturer
    CARDINAL HEALTH MEDICAL PRODUCTS AND SERVICES
    Product Code
    KDQ
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    THORACENTESIS/PARACENTESIS KIT OPENED, AND NEEDLE IN KIT WAS BENT. UNABLE TO USE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * KIT, THORACENTESIS KDQ CARDINAL HEALTH MEDICAL PRODUCTS AND SERVICES * L8A240

    Patients

    Seq Age Sex Outcome Treatment
    1 *