BEUDAMED
    FDA Adverse Event Death Summary report: N

    TUCKER-MCLEAN FORCEPS

    MDR report key: 14516 · Received June 2, 1994

    Report

    Report Number
    14516
    Event Type
    Death
    Date Received
    June 2, 1994
    Date of Event
    May 19, 1994
    Report Date
    May 31, 1994
    Manufacturer
    V. MUELLER DIV. BAXTER HEALTHCARE CORP.
    Product Code
    HDA
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    CO, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    SECOND TWIN OF 40 WEEK GESTATION, REQUIRED APPLICATION OF TWO PAIRS OF FORCEPS WITHOUT SUCCESS. BABY SUCCESSFULLY EXTRACTED WITH ANOTHER FORCEPS. BABY WITH NO HEARTBEAT AT BIRTH. RESUSCITATION EFFORTS UNSUCCESSFUL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TUCKER-MCLEAN FORCEPS ABSTETRICAL FORCEPS HDA V. MUELLER DIV. BAXTER HEALTHCARE CORP.

    Patients

    Seq Age Sex Outcome Treatment
    1 0 DAY Death