BEUDAMED
    FDA Adverse Event Other Summary report: N

    OCEAN WATER SEAL CHEST DRAINAGE

    MDR report key: 1310532 · Received February 9, 2009

    Report

    Report Number
    MW5009927
    Event Type
    Other
    Date Received
    February 9, 2009
    Date of Event
    December 21, 2008
    Report Date
    February 9, 2009
    Manufacturer
    ATRIUM MEDICAL CORP
    Product Code
    KDQ
    Report Source
    Voluntary report
    Reporter Location
    NY, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    DEVICE TUBING FROM PATIENT CHEST TUBE TO DRAINAGE, SYSTEM MAY BE TOO PLIABLE AND IS ABLE TO BE TOTALLY OCCLUDED WHERE KINKED BENEATH PATIENT LYING ON IT, AND MAY GO UNDETECTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OCEAN WATER SEAL CHEST DRAINAGE CHEST TUBE DRAINAGE SYSTEM KDQ ATRIUM MEDICAL CORP

    Patients

    Seq Age Sex Outcome Treatment
    1