BEUDAMED
    FDA Adverse Event Other Summary report: N

    LYTIC AGENT DIFF-SCREEN

    MDR report key: 53056 · Received November 27, 1996

    Report

    Report Number
    2919069-1996-00001
    Event Type
    Other
    Date Received
    November 27, 1996
    Date of Event
    October 31, 1996
    Report Date
    November 27, 1996
    Manufacturer
    ABBOTT DIAGNOSTICS DIV/CELLDYN
    Product Code
    GGK
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    ON 10/31/96, A LABORATORY TECHNICIAN AT THE ACCOUNT SPLASHED LYSE REAGENT INTO HER EYE, WHILE POURING IT INTO A CONTAINER. THE LABORATORY TECHNICIAN WAS NOT WEARING GOGGLES WHEN SHE WAS POURING THE REAGENT. SHE DID SEEK MEDICAL ATTENTION AND THERE IS NO REPORT OF INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LYTIC AGENT DIFF-SCREEN CELL-DYN LYSE REAGENT GGK ABBOTT DIAGNOSTICS DIV/CELLDYN NA 1960012

    Patients

    Seq Age Sex Outcome Treatment
    1 31 YR Other