BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® COMPACT TEST DRUM

    MDR report key: 1863992 · Received October 11, 2010

    Report

    Report Number
    1823260-2010-06055
    Event Type
    Malfunction
    Date Received
    October 11, 2010
    Date of Event
    October 7, 2010
    Report Date
    October 26, 2010
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K031755
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    PATIENT

    Narratives

    Additional Manufacturer Narrative · 1

    IT WAS UNKNOWN IF THE INITIAL REPORTER SENT REPORT TO THE FDA.

    Description of Event or Problem · 1

    INFORMATION RECEIVED INDICATES THE SIDERAIL IS HANGING ON THE BED BY THE TWO OUTER SIDERAILS AND WILL NOT GO UP INTO THE LATCH POSITION.

    Description of Event or Problem · 1

    REPORTER ALLEGED OBTAINING THE RESULTS OF 199 MG/DL, 237 MG/DL AND 71 MG/DL BACK TO BACK WITHIN 10 MINUTES ON THE COMPACT PLUS SYSTEM. REPORTER STATED THAT HE TOOK HIS 100 MG OF JANUVIA AS NORMAL AFTER TESTING. NO OTHER ACTIONS WERE REPORTED TAKEN OR TREATMENT RECEIVED. 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 ® COMPACT TEST DRUM BLOOD GLUCOSE MONITORING TEST STRIPS LFR ROCHE DIAGNOSTICS 20726741

    Patients

    Seq Age Sex Outcome Treatment
    1 088 YR JANUVIA| FLOMAX| LEXAPRO| ALPRAZOLAM| LISINOPRIL| NORVASC| PLAVIX| BLOOD PRESSURE MACHINE