BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TINCOCO

    MDR report key: 2172038 · Received July 14, 2011

    Report

    Report Number
    MW5021417
    Event Type
    Malfunction
    Date Received
    July 14, 2011
    Date of Event
    July 12, 2011
    Report Date
    July 14, 2011
    Product Code
    DWL
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I HAD BOUGHT A TINCOCO COMPRESSION LEGWEAR WHICH DOES NOT FIT THE DESCRIPTION, IT DOES NOT "TIGHT" AS NORMAL LIKE SOCKS. BUT THE SELLER CLAIM THAT IT IS REAL AND REFUSE TO REFUND OR CHANGE GOOD TO ME. THIS IS MY SECOND TIME TO BUY TINCOCO. FIRST TIME WAS WITH ANOTHER PERSON, IT IS GOOD TO WEAR AND VERY TIGHT, BUT THIS SECOND TIME WITH ANOTHER SELLER, LEFT ME DISAPPOINTED AND SAD. DATES OF USE: (B)(6) 2011.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TINCOCO TINCOCO COMPRESSION LEGWEAR 980D DWL JY-1066 ???

    Patients

    Seq Age Sex Outcome Treatment
    1 25 YR Other