BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® COMPACT TEST DRUM

    MDR report key: 2220271 · Received August 23, 2011

    Report

    Report Number
    1823260-2011-04448
    Event Type
    Malfunction
    Date Received
    August 23, 2011
    Date of Event
    July 18, 2011
    Report Date
    September 28, 2011
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K031755
    Removal / Correction Number
    NA
    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

    CUSTOMER REPORTEDLY RECEIVED THE FOLLOWING RESULTS ON THE COMPACT PLUS SYSTEM WITHIN 10 MINUTES: 1. 170 MG/DL AND 70 MG/DL - WITHIN 1-2 MINUTES 2. 200 MG/DL AND 80 MG/DL - WITHIN 1-2 MINUTES 3. 140 MG/DL AND 70 MG/DL - WITHIN 1-2 MINUTES SETS OF READINGS WERE TAKEN ON DIFFERENT DAYS. NO ACTIONS TAKEN BASED ON DEVICE RESULTS. NO ADVERSE EVENT REPORTED. REQUESTED RETURN OF SUSPECT DEVICE AND REPLACEMENT WAS SENT.

    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 NA 20729846

    Patients

    Seq Age Sex Outcome Treatment
    1 048 YR ZOCOR| COZAAR| BONIVA| VITAMIN D| FOLIC ACID| NORVASC| NOVOLOG| LANTUS| FISH OIL