BEUDAMED
    FDA Adverse Event Other Summary report: N

    GLOVE,SURGICAL,LATEX,POWDER FREE

    MDR report key: 532609 · Received March 4, 2004

    Report

    Report Number
    1417592-2004-00003
    Event Type
    Other
    Date Received
    March 4, 2004
    Date of Event
    February 2, 2004
    Report Date
    March 2, 2004
    Manufacturer
    MEDLINE INDUSTRIES, INC.
    Product Code
    KGO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    A NURSE HAD A REACTION WHILE WEARING A LATEX SURGICAL GLOVE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GLOVE,SURGICAL,LATEX,POWDER FREE LATEX SURGICAL GLOVE KGO MEDLINE INDUSTRIES, INC. MDS108070 2206273

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other