BEUDAMED
    FDA Adverse Event Injury Summary report: N

    STEP VERRES NEEDLE AND TROCAR

    MDR report key: 21602 · Received May 1, 1995

    Report

    Report Number
    MW1005778
    Event Type
    Injury
    Date Received
    May 1, 1995
    Date of Event
    March 28, 1995
    Report Date
    March 31, 1995
    Manufacturer
    INNERDYNE MEDICAL
    Product Code
    FHP
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NV, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PENETRATED BOWEL WALL OF PT WHEN USING NEEDLE AND TROCAR. (ALSO SEE 1005777.)

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STEP VERRES NEEDLE AND TROCAR VERRES NEEDLE AND TROCAR FHP INNERDYNE MEDICAL S10000D, S101012 9502002, 9501033

    Patients

    Seq Age Sex Outcome Treatment
    1 * Hospitalization