BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNK

    MDR report key: 193224 · Received October 19, 1998

    Report

    Report Number
    1520348-1998-00189
    Event Type
    Injury
    Date Received
    October 19, 1998
    Date of Event
    September 1, 1994
    Report Date
    October 9, 1998
    Manufacturer
    SMITH & NEPHEW PERRY
    Product Code
    LYY
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Description of Event or Problem · 1

    THE LAWSUIT ALLEGES THAT ON OR ABOUT 10/1994 THE PLAINTIFF BECAME AWARE THAT SYMTOMS SHE WAS SUFFERING WERE DUE TO HER EXPOSURE TO LATEX PRODUCTS.

    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