BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® COMPACT TEST DRUM

    MDR report key: 3190617 · Received June 26, 2013

    Report

    Report Number
    1823260-2013-03862
    Event Type
    Malfunction
    Date Received
    June 26, 2013
    Date of Event
    May 26, 2013
    Report Date
    July 31, 2013
    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

    CALLER REPORTED COMPACT PLUS SYSTEM BLOOD GLUCOSE RESULTS 335 MG/DL AND 33 MG/DL WITHIN 10 MINUTES. NO ADVERSE EVENT WAS REPORTED. A REQUEST WAS MADE FOR THE RETURN OF THE METER AND STRIPS, REPLACEMENT SENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    290040 ACCU-CHEK ® COMPACT TEST DRUM BLOOD GLUCOSE MONITORING TEST STRIPS LFR ROCHE DIAGNOSTICS NA ASKU

    Patients

    Seq Age Sex Outcome Treatment
    1 072 YR METFORMIN 2 TIMES A DAY| GABAPENTIN 4X DAY| NEXIUM 1XDAY| AMLODIPINE 1XDAY| LISINOPRIL 2XDAY| LEXAPRO 1XDAY| LASIX| CANE| PRAVASTATIN 1XDAY| WALKER| LANTUS 2XDAY| OXYGEN| CARVATALOG 2XDAY