BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ALPHA I

    MDR report key: 771560 · Received October 20, 2006

    Report

    Report Number
    2125050-2006-00305
    Event Type
    Injury
    Date Received
    October 20, 2006
    Date of Event
    May 30, 2006
    Report Date
    September 20, 2006
    Manufacturer
    COLOPLAST MANUFACTURING US, LLC
    Product Code
    FHW
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SC, US
    Reporter Occupation
    NURSE

    Narratives

    Additional Manufacturer Narrative · 1

    AN EVALUATION IS PENDING THE DECONTAMINATION OF THE COMPONENT(S). AN EVALUATION WILL BE FORWARDED UPON COMPLETION.

    Description of Event or Problem · 1

    ACCORDING TO THE INFORMATION THERE WAS A MALFUNCTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ALPHA I INFLATABLE PENILE PROSTHESIS FHW COLOPLAST MANUFACTURING US, LLC NI NI

    Patients

    Seq Age Sex Outcome Treatment
    1 74 YR Hospitalization| R