BEUDAMED
    FDA Adverse Event Other Summary report: N

    GLOVE TRIFLEX 6.5 PWD LATEX SURG

    MDR report key: 654451 · Received December 15, 2005

    Report

    Report Number
    1423507-2005-00147
    Event Type
    Other
    Date Received
    December 15, 2005
    Date of Event
    November 17, 2005
    Report Date
    December 15, 2005
    Manufacturer
    CARDINAL HEALTH
    Product Code
    KGO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    DURING PROCEDURE IN CATH LAB, THUMB OF GLOVE TORE. NO BLOOD WORK WAS DONE. DR ORDERED 1GM OF ANCEF FOR THE PATIENT BECAUSE THE GLOVE TORE. ANTIBIOTIC WAS GIVEN TO THE PATIENT DURING THE PROCEDURE WHILE THEY WERE STILL ON THE TABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GLOVE TRIFLEX 6.5 PWD LATEX SURG SURGEON'S GLOVE KGO CARDINAL HEALTH * PS05H049

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other