BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK ® SPIRIT COMBO

    MDR report key: 4251402 · Received November 14, 2014

    Report

    Report Number
    1823260-2014-08927
    Event Type
    Malfunction
    Date Received
    November 14, 2014
    Date of Event
    August 25, 2014
    Report Date
    December 22, 2014
    Manufacturer
    ROCHE DIAGNOSTICS
    Product Code
    LZG
    PMA / PMN Number
    NA
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Additional Manufacturer Narrative · 1

    THE EVENT OCCURRED IN (B)(6). WHILE THIS PRODUCT IS NOT SOLD IN THE UNITED STATES, IT IS LIKE OR SIMILAR TO A PRODUCT MARKETED IN THE UNITED STATES.

    Description of Event or Problem · 1

    PATIENT REPORTED HAVING CONCERN WITH THE PUMP. PATIENT STATED THE PUMP DISPLAY A W2 (BATTERY LOW) ERROR MESSAGE AND A LITTLE LATER SWITCHED OFF WITHOUT DISPLAYING THE E2 (BATTERY DEPLETED) ERROR MESSAGE. PATIENT STATED THE PUMP GAVE AN ACOUSTIC ALERT WITHOUT DISPLAYING AN ERROR MESSAGE. NO ADVERSE EVENT REPORTED. REQUESTED RETURN OF THE ALLEGED PUMP FOR EVALUATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    737472 ACCU-CHEK ® SPIRIT COMBO INSULIN INFUSION PUMP LZG ROCHE DIAGNOSTICS NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 049 YR