BEUDAMED
    FDA Adverse Event Injury Summary report: N

    WECK

    MDR report key: 3010675 · Received March 12, 2013

    Report

    Report Number
    MW5029367
    Event Type
    Injury
    Date Received
    March 12, 2013
    Date of Event
    March 11, 2013
    Report Date
    March 12, 2013
    Manufacturer
    PILLING WECK
    Product Code
    HHK
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    #2 WECK CURETTE INTRODUCED INTO UTERUS DURING D&C. CURETTE WAS RETRIEVED AND NOTED TO BE MISSING LOOP END. XRAY PERFORMED AND FOREIGN BODY NOT SEEN. TIP FOUND IN PLASTIC GYN BAG BY CIRCULATING NURSE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    104455 WECK CURRETTE #2 HHK PILLING WECK

    Patients

    Seq Age Sex Outcome Treatment
    1 48 YR Hospitalization