BEUDAMED
    FDA Adverse Event Other Summary report: N

    LIQUICHEK IMMUNOASSAY PLUS

    MDR report key: 313904 · Received January 19, 2001

    Report

    Report Number
    2016706-2001-00001
    Event Type
    Other
    Date Received
    January 19, 2001
    Date of Event
    December 5, 2000
    Report Date
    January 19, 2001
    Manufacturer
    BIO-RAD LABORATORIES
    Product Code
    JJT
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    CUSTOMER STUCK SELF WITH A SYRINGE CONTAINING PRODUCT FROM LEVEL 2 OR 3 OF LIQUICHEK IMMUNOASSAY PLUS. CUSTOMER REPORTED INCIDENT TO TECHNICAL SERVICES. INCIDENT WAS FORWARDED TO REGULATORY AFFAIRS FOR FOLLOW-UP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2659 LIQUICHEK IMMUNOASSAY PLUS MULTI-ANALYTE CONTROL (ASSAYED/UNASSAYED) JJT BIO-RAD LABORATORIES UNK 40570

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other