BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNK

    MDR report key: 39187 · Received September 20, 1996

    Report

    Report Number
    1520348-1996-00008
    Event Type
    Injury
    Date Received
    September 20, 1996
    Report Date
    September 9, 1996
    Manufacturer
    SMITH & NEPHEW PERRY
    Product Code
    LYY
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Description of Event or Problem · 1

    THE AFFECTED INDIVIDUAL CLAIMS HE/SHE DEVELOPED SEVERE ILLNESSES AND INJURIES TO SKIN SUCH DISCOLORATION, SORENESS, RASHES, RESPIRATORY AND /OR OTHER RELATED DISEASES, DISORDERS AND REACTIONS ALLEGEDLY CAUSED BY EXTENDED EXPOSURE TO THE CHEMICAL SUBSTANCES OF THE GLOVES. CLAIMS ARE AGAINST MULTIPLE MFRS INCLUDING UNKNOWN ONES AND IT IS NOT CURRENTLY KNOWN WHOSE GLOVES WERE INVOLVED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UNK LATEX GLOVES LYY SMITH & NEPHEW PERRY UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other