BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DEXON II 2-0 36" BEIGE C-9

    MDR report key: 225319 · Received May 25, 1999

    Report

    Report Number
    2648188-1999-00014
    Event Type
    Malfunction
    Date Received
    May 25, 1999
    Report Date
    April 28, 1999
    Manufacturer
    KENDALL HEALTHCARE PRODUCTS CO
    Product Code
    GAN
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE SUTURE WAS USED DURING AN UNSPECIFIED PROCEDURE BY THE VETERINARIAN. REPORTEDLY, THE SUTURE CAUSED AN ABSCESS RESULTING IN THE DEATH OF A CAT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DEXON II 2-0 36" BEIGE C-9 Implant SYNTHETIC ABSORBABLE SUTURE GAN KENDALL HEALTHCARE PRODUCTS CO NA 971034

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN