BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® COMPACT TEST DRUM

    MDR report key: 1971839 · Received January 27, 2011

    Report

    Report Number
    1823260-2011-00487
    Event Type
    Malfunction
    Date Received
    January 27, 2011
    Date of Event
    January 17, 2011
    Report Date
    March 21, 2011
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LFR
    PMA / PMN Number
    K031755
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    CUSTOMER REPORTEDLY RECEIVED THE FOLLOWING RESULTS ON THE COMPACT PLUS SYSTEM WITHIN 10 MINUTES: HI (GREATER THAN 600 MG/DL) AND 147 MG/DL. 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 20727545

    Patients

    Seq Age Sex Outcome Treatment
    1 045 YR METHADONE| METOPROLOL| XANAX| ZANTAC| POTASSIUM| PLAVIX 1X DAILY| PHENERGAN| ISOSORBIDE 1X DAILY| ASPIRIN| BLOOD PRESSURE METER| WHEELCHAIR| LANTUS| ATENOLOL| CREON| LIPITOR| NITROGLYCERINE| LASIX| NOVOLOG