BEUDAMED
    FDA Adverse Event Other Summary report: N

    ORTHO ELISA BAR CODE READER II

    MDR report key: 279680 · Received May 24, 2000

    Report

    Report Number
    2250051-2000-00062
    Event Type
    Other
    Date Received
    May 24, 2000
    Date of Event
    May 3, 2000
    Report Date
    May 3, 2000
    Manufacturer
    INTERMEC CORP./GREENBROOK CORPORATE CENTER
    Product Code
    LRH
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Location
    MI, US

    Narratives

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED WHILE USING A HAND HELD INTERMEC BARCODE WAND, IT READ A SAMPLE BARCODE INCORRECTLY AS "184613865" INSTEAD OF "018GK13865". NO DEATH OR SERIOUS INJURY WAS ASSOCIATED WITH THIS EVENT. THIS REPORT CORRESPONDS TO ORTHO-CLINICAL DIAGNOSTICS COMPLAINT NUMBER 00-02186-05.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ORTHO ELISA BAR CODE READER II BAR CODE READER LRH INTERMEC CORP./GREENBROOK CORPORATE CENTER 9720C01,D01,E01,F01 NA

    Patients

    Seq Age Sex Outcome Treatment
    1