BEUDAMED
    FDA Adverse Event Summary report: N

    CYTOSPIN CYTOCENTRIFUGE

    MDR report key: 23175 · Received July 3, 1995

    Report

    Report Number
    MW1006390
    Date Received
    July 3, 1995
    Manufacturer
    SANDON INC.
    Product Code
    JQC
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    THE FUNNELS ARE CONTAMINATED WITH BACTERIA AND CAUSE DIAGNOSTIC PROBLEMS WHEN USED WITH NORMALLY-STERILE BODY FLUIDS.

    Description of Event or Problem · 1

    THE FUNNELS ARE CONTAMINATED WITH BACTERIA AND CAUSE DIAGNOSTIC PROBLEMS WHEN USED WITH NORMALLY-STERILE BODY FLUIDS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CYTOSPIN CYTOCENTRIFUGE Implant CYTOCENTRIFUGE JQC SANDON INC. CYTOSPIN 3 MANY

    Patients

    Seq Age Sex Outcome Treatment
    1 *