BEUDAMED
    FDA Adverse Event Injury Summary report: N

    INTERMITTENT MAGIC3

    MDR report key: 5068602 · Received September 10, 2015

    Report

    Report Number
    1018233-2015-00338
    Event Type
    Injury
    Date Received
    September 10, 2015
    Date of Event
    August 12, 2015
    Report Date
    August 17, 2015
    Manufacturer
    ROCHESTER MEDICAL CORP 2130787
    Product Code
    KOD
    PMA / PMN Number
    K000723
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    PATIENT

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE WAS NOT RETURNED FOR EVALUATION. THE LOT NUMBER IS UNKNOWN, THEREFORE THE DEVICE HISTORY RECORD COULD NOT BE REVIEWED. THE INSTRUCTIONS FOR USE STATES THE FOLLOWING: "HOW TO PREPARE AND USE THE MAGIC 3 CATHETER. THE CATHETER IS INTENDED FOR URINARY BLADDER DRAINAGE IN PATIENTS REQUIRING CATHETERIZATION FOR MANAGEMENT OF INCONTINENCE, VOIDING DYSFUNCTION, AND SURGICAL PROCEDURES. THIS IS A SINGLE USE DEVICE. DO NOT REUSE. REUSE OF A SINGLE USE DEVICE INCREASES THE RISK OF CATHETER ACQUIRED URINARY TRACT INFECTIONS. URETHRAL CATHETER FOR UROLOGICAL USE ONLY. DISCARD AFTER USE, DO NOT RESTERILIZE. MADE OF SILICONE ELASTOMER." DESPITE GOOD FAITH EFFORTS TO OBTAIN ADDITIONAL INFORMATION, THE COMPLAINANT / REPORTER WAS UNABLE OR UNWILLING TO PROVIDE ANY FURTHER PATIENT, PRODUCT, OR PROCEDURAL DETAILS TO BARD.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE PATIENT ALLEGEDLY EXPERIENCED A URINARY TRACT INFECTION AS A RESULT OF USING THE DEVICE. PER ADDITIONAL INFORMATION RECEIVED THE PATIENT WAS PRESCRIBED GENLAMICIN AND SALINE TO TREAT THE INFECTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    598461 INTERMITTENT MAGIC3 MAGIC 3 KOD ROCHESTER MEDICAL CORP 2130787 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 43 Required Intervention