BEUDAMED
    FDA Adverse Event Other Summary report: N

    LIQUICHEK URINALYSIS CONTROL

    MDR report key: 5353669 · Received September 7, 2004

    Report

    Report Number
    2016706-2004-00001
    Event Type
    Other
    Date Received
    September 7, 2004
    Date of Event
    August 12, 2004
    Report Date
    August 17, 2004
    Manufacturer
    BIO-RAD LABORATORIES
    Product Code
    JJW
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    Reporter Occupation
    0

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICAL SERVICES RECEIVED THE INITIAL REPORT AND EXPLAINED TO THE LAB PROFESSIONAL SHE SHOULD FOLLOW HER LAB'S PROCEDURE FOR INJURY AND POTENTIAL HAZARDOUS MATERIALS EXPOSURE.

    Description of Event or Problem · 1

    A LAB PROFESSIONAL SPLASHED LEVEL 2, URINALYSIS CONTROL IN HER RIGHT EYE ON (B)(6) 2004 AT 3 A. M.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LIQUICHEK URINALYSIS CONTROL QUALITY CONTROL MATERIAL JJW BIO-RAD LABORATORIES NA 61202

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Other