BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® AVIVA TEST STRIPS

    MDR report key: 1863851 · Received October 11, 2010

    Report

    Report Number
    1823260-2010-06035
    Event Type
    Malfunction
    Date Received
    October 11, 2010
    Date of Event
    October 6, 2010
    Report Date
    October 15, 2010
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K043474
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    PATIENT

    Narratives

    Additional Manufacturer Narrative · 1

    IT WAS UNKNOWN IF THE INITIAL REPORTER SENT REPORT TO THE FDA. THIS MEDWATCH REPORT IS FOR THE SUSPECT DEVICE USED IN SYSTEM 2. (B)(4).

    Description of Event or Problem · 1

    IT WAS REPORTED THAT "CUP WAS IMPLANTED WHEN THE PT WAS A CHILD AND SINCE HAS OUTGROWN HIS IMPLANTS - NOTHING WAS WRONG WITH THE IMPLANTS."

    Description of Event or Problem · 1

    REPORTER ALLEGED OBTAINING A RESULT OF 399 MG/DL ON AVIVA SYSTEM 1 COMPARED BACK TO BACK WITH A RESULT OF 170 MG/DL ON AVIVA SYSTEM 2 WHEN TESTING WAS PERFORMED WITHIN 10 MINUTES. NO ACTIONS WERE REPORTED TAKEN OR TREATMENT RECEIVED. REPORTER STATED THAT SHE DID NOT PREPARE HER HANDS PRIOR TO OBTAINING THE READING. NO ADVERSE EVENT REPORTED. A REQUEST WAS MADE FOR THE RETURN OF THE AFFECTED PRODUCT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACCU-CHEK ® AVIVA TEST STRIPS BLOOD GLUCOSE MONITORING TEST STRIPS LFR ROCHE DIAGNOSTICS NA 302801

    Patients

    Seq Age Sex Outcome Treatment
    1 077 YR