BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    QUICK SET PARADIGM

    MDR report key: 1522115 · Received November 2, 2009

    Report

    Report Number
    8021545-2009-00016
    Event Type
    Malfunction
    Date Received
    November 2, 2009
    Date of Event
    July 3, 2009
    Report Date
    October 28, 2009
    Manufacturer
    UNOMEDICAL A/S
    Product Code
    FPA
    PMA / PMN Number
    K991759
    Removal / Correction Number
    Z-1705-2009
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    EVALUATION SUMMARY: TWO USED DEVICES WERE RETURNED FOR EVALUATION. USED DEVICES: THE TUBING WAS VISUALLY INSPECTED FOR ANY TEARS OR CRACKS ON THE TUBING IT SELF AND ON THE ATTACHED CONNECTOR PARTS. FURTHERMORE A FLOW TEST A P-CAP CONNECTOR VENT TEST WERE PERFORMED. THE MEMBRANES IN THE P-CAP CONNECTORS WERE HUMID AND BOTH SAMPLES ALSO FAILED THE P-CAP CONNECTOR VENT TEST. FURTHERMORE ONE USED SAMPLE FAILED THE FLOW TEST OF THE TUBING. REFERENCE SAMPLES: THE REFERENCE MATERIAL WAS TESTED AND ALL SAMPLES WERE FOUND TO BE WITHIN SPECIFICATIONS. A REVIEW OF THE RELEVANT DEVICE HISTORY RECORDS AND A SEARCH FOR RELEVANT DEVIATIONS OR SIMILAR COMPLAINTS RELATED TO THE SPECIFIC DEVICE RESULTED IN 3 SIMILAR COMPLAINTS FOR THE INVOLVED LOT NUMBER 8200954. NO RELEVANT DEVIATIONS DURING MANUFACTURING WERE RECORDED.

    Description of Event or Problem · 1

    PATIENT STATES THAT SHE HAS OBSERVED INSULIN SQUIRTING OUT OF THE TUBING ON 2 DIFFERENT INFUSION SETS DURING PRIMING. THE MALFUNCTION WAS SOLVED BY CHANGING INFUSION SET. THE MALFUNCTION OCCURRED PRIOR TO USE. UNOMEDICAL RECEIVED THE COMPLAINT THROUGH (B) (4), THE DISTRIBUTOR OF THE INFUSION SET. (B) (4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 QUICK SET PARADIGM FPA UNOMEDICAL A/S MMT-397 8200954

    Patients

    Seq Age Sex Outcome Treatment
    1 NA