BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    QUICK SET PARADIGM

    MDR report key: 1526480 · Received November 2, 2009

    Report

    Report Number
    8021545-2009-00028
    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

    EVAL SUMMARY: TWO USED DEVICES WERE RETURNED FOR EVAL. USED DEVICES: THE TUBING WAS VISUALLY INSPECTED FOR ANY TEARS OR CRACKS ON THE TUBING ITSELF AND ON THE ATTACHED CONNECTOR PARTS. FURTHERMORE, A FLOW TEST AND 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 AND THE FLOW TEST OF THE TUBING. UNUSED DEVICES: NO UNUSED DEVICES RETURNED FOR EVAL. REFERENCE SAMPLES: THE REFERENCE MATERIAL WAS TESTED AND 1 SAMPLE HAD A HUMID P-CAP CONNECTOR MEMBRANE. THE SAMPLE FAILED THE P-CAP CONNECTOR VENT TEST. THE REMAINING 9 SAMPLES WERE FOUND TO BE WITHIN SPECS. A REVIEW OF THE RELEVANT DEVICE HISTORY RECORDS AND A SEARCH FOR RELEVANT DEVIATIONS OR SIMILAR COMPLAINTS RELATED TO THE SPECIFIC DEVICE RESULTED IN NO SIMILAR COMPLAINTS FOR THE INVOLVED LOT NUMBER 8200805. NO RELEVANT DEVIATIONS DURING MFG WERE RECORDED. (B)(4)

    Description of Event or Problem · 1

    PT STATES THAT INSULIN IS EXITING THE TUBING BUT THE FLOW IS NOT RECORDED BY PUMP DURING PRIMING OF INFUSION SET. MALFUNCTION OCCURRED PRIOR TO USE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 QUICK SET PARADIGM FPA UNOMEDICAL A/S MMT-397 8200805

    Patients

    Seq Age Sex Outcome Treatment
    1 NA