BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCU-CHEK FLEXLINK PLUS

    MDR report key: 2013042 · Received March 4, 2011

    Report

    Report Number
    2183996-2011-00437
    Event Type
    Malfunction
    Date Received
    March 4, 2011
    Date of Event
    February 15, 2011
    Report Date
    February 25, 2011
    Manufacturer
    ROCHE INSULIN DELIVERY SYSTEMS, INC.
    Product Code
    LZG
    PMA / PMN Number
    NA
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THIS INCIDENT OCCURRED OUTSIDE THE UNITED STATES. INFO CONTAINED WITHIN THIS REPORT IS ALL THAT IS AVAILABLE AT THIS TIME. IF FURTHER INFO IS OBTAINED, IT WILL BE PROVIDED IN THE SUPPLEMENTAL REPORT. NO PRODUCT WILL BE RETURNED FOR EVAL.

    Description of Event or Problem · 1

    THE PT REPORTED THE INFUSION SITE WAS CHANGED ON (B)(6) 2011. ON (B)(6) 2011, SHE WOKE UP AND FELT NAUSEOUS AND SHE VOMITED. HER BLOOD GLUCOSE MEASURED 600 MG/DL AND SHE FOUND THE INFUSION SITE CANNULA WAS BENT. SHE ALSO REPORTED THE INFUSION TUBING HAS BECOME SEPARATED FROM THE HEADSET. NO FURTHER INFO IS AVAILABLE. THE PT DID NOT REQUIRE TREATMENT FROM A HEALTH CARE PROFESSIONAL OR SECOND PARTY TO ADDRESS THE ISSUE. THE ALLEGED PRODUCT WAS DISCARDED. NO PRODUCT WILL BE RETURNED FOR EVAL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACCU-CHEK FLEXLINK PLUS INSULIN INFUSION SET LZG ROCHE INSULIN DELIVERY SYSTEMS, INC. NA GWX105

    Patients

    Seq Age Sex Outcome Treatment
    1 39 YR INSULIN INFUSION PUMP| INSULIN