BEUDAMED
    FDA Adverse Event Other Summary report: N

    LIQUICHEK URINALYSIS CONTROL

    MDR report key: 466589 · Received June 13, 2003

    Report

    Report Number
    2016706-2003-00002
    Event Type
    Other
    Date Received
    June 13, 2003
    Date of Event
    May 13, 2003
    Report Date
    May 15, 2003
    Manufacturer
    BIO-RAD LABORATORIES
    Product Code
    JJT
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IS
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    A LAB TECH CAME INTO CONTACT WITH THE PRODUCT WHEN THE TECHNICIAN'S FINGER WAS STUCK BY A NEEDLE. THE LAB TECH USED THE SYRINGE TO REMOVE THE CONTROL FROM THE VIAL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LIQUICHEK URINALYSIS CONTROL QUALITY CONTROL MATERIAL JJT BIO-RAD LABORATORIES NA 61160

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other