BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MEDICAL ACTION INDUSTRIES, INC.

    MDR report key: 489088 · Received September 26, 2003

    Report

    Report Number
    MW1029678
    Event Type
    Malfunction
    Date Received
    September 26, 2003
    Report Date
    September 25, 2003
    Manufacturer
    MEDICAL ACTION INDUSTRIES
    Product Code
    LRW
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    UT, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    STERILE PACKAGE-RUST ON STERILE PACKAGED SCISSORS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MEDICAL ACTION INDUSTRIES, INC. STERILE SHARP/BLUNT SCISSORS LRW MEDICAL ACTION INDUSTRIES * 66233
    2 MEDICAL ACTION INDUSTRIES INC STERILE SHARP/BLUNT SCISSORS LRW MEDICAL ACTION INDUSTRIES * 57058
    3 MEDICAL ACTION INDUSTRIES INC STERILE SHARP/BLUNT SCISSORS LRW MEDICAL ACTION INDUSTRIES * 66835

    Patients

    Seq Age Sex Outcome Treatment
    1 *