BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PERSONA SURGICAL BLADE 15

    MDR report key: 837451 · Received April 4, 2007

    Report

    Report Number
    837451
    Event Type
    Malfunction
    Date Received
    April 4, 2007
    Date of Event
    March 28, 2007
    Report Date
    April 4, 2007
    Manufacturer
    AMERICAN SAFETY RAZOR CO.
    Product Code
    GES
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    IA, US

    Narratives

    Description of Event or Problem · 1

    OR PERSONNEL REPORTED PERSONA SURGICAL BLADE #15 HAD DOUBLE BLADES IN THEM. ONLY LOT AFFECTED TO DATE IS 2012-02EB.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PERSONA SURGICAL BLADE 15 BLADE, SURGICAL GES AMERICAN SAFETY RAZOR CO. MFR 73-0415 2012-02EB

    Patients

    Seq Age Sex Outcome Treatment
    1 *