BEUDAMED
    FDA Adverse Event Other Summary report: N

    ASPEN SURGICAL PRODUCTS

    MDR report key: 479262 · Received August 22, 2003

    Report

    Report Number
    479262
    Event Type
    Other
    Date Received
    August 22, 2003
    Date of Event
    July 17, 2003
    Report Date
    August 12, 2003
    Manufacturer
    ASPEN SURGICAL PRODUCTS
    Product Code
    GAB
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    CA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PHYSICIAN WAS USING A MAYO NEEDLE TO SUTURE AFFECTED AREA. EYE OF THE NEEDLE BROKE OFF FROM THE BODY OF THE NEEDLE AND WAS NOT LOCATED. AFFECTED AREA IS SUBCUTANEOUS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ASPEN SURGICAL PRODUCTS MARTINS UTERINE #5 GAB ASPEN SURGICAL PRODUCTS * 2007-03-19

    Patients

    Seq Age Sex Outcome Treatment
    1 84 YR Other