BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MEDTRONIC EXTENDED

    MDR report key: 19284990 · Received May 10, 2024

    Report

    Report Number
    8021545-2024-00323
    Event Type
    Malfunction
    Date Received
    May 10, 2024
    Report Date
    July 24, 2024
    Product Code
    FPA
    UDI-DI
    05705244022836
    PMA / PMN Number
    K210544
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER
    Health Professional
    N

    Narratives

    Additional Manufacturer Narrative · 0

    MDR 8021545-2024-00323 - DEVICE 3 OF 4.

    Additional Manufacturer Narrative · 0

    SUPPLEMENTAL REPORT 01 - MDR 1858715 - MDR 8021545-2024-00323. ADDITIONAL INFORMATION - THIS MDR IS BEING SUBMITTED TO INCLUDE THE BELOW: H6: INVESTIGATION RESULTS UNDER TYPE OF INVESTIGATION, INVESTIGATION FINDINGS, INVESTIGATION CONCLUSIONS. H11: INVESTIGATION SUMMARY: THE FOLLOWING TESTS WERE COMPLETED FOR 5 REFERENCE SAMPLES AND 4 RETURNED USED DEVICES (1 TUBING AND 3 SETS) OF LOT: 6003163: 1. VISUAL INSPECTION. 5 REFERENCE SAMPLES, 1 USED TUBING AND 3 USED SETS WERE VISUALLY INSPECTED AND NO DAMAGES OR BENT. 2. 4802011, FLOW TEST ON CUSTOMER COMPLAINTS -PRUEBAS DE FLUJO EN QUEJAS DEL CLIENTE, VERSION 10. 5 REFERENCE SAMPLES, 1 USED SET AND 1 USED TUBING MET THE CRITERIA OF MINIMUM 30ML/MINUTE BUT IN 2 USED SETS THE P-CAP CONNECTOR NEEDLE WAS CLOGGED (BY INSULIN). 3. 4802112 LEAK TEST IN WATER, VERSION 44. 5 REFERENCE SAMPLES, 3 USED SETS AND 1 USED TUBING NO AIR BUBBLES BURSTING DURING THE TEST TIME OF 30 SECONDS. FLOW TEST VALUES ON RETURNED USED DEVICES: P2: 53, P4: 65. FLOW TEST VALUES ON REFERENCE SAMPLES: P1: 45, P2: 58, P3: 47, P4: 52, P5: 45.

    Description of Event or Problem · 0

    UNOMEDICAL REFERENCE NUMBER (B)(4). EVENT OCCURRED IN THE UNITED STATES. ON 09-APR-2024, IT WAS REPORTED THAT THE PATIENT FACED LEAKAGE AT SITE ON (B)(6) 2024. MOREOVER, THE ISSUE OCCURED WITH FOUR INFUSION SETS USED FOR ONE TO TWO DAYS. NO FURTHER INFORMATION WAS AVAILABLE.

    Description of Event or Problem · 0

    TO DATE NO ADDITIONAL PATIENT OR EVENT DETAILS HAVE BEEN RECEIVED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2123089 MEDTRONIC EXTENDED UNO EWIS BLUE 80/9 HCAP 10PK INT FPA 6003163 05705244022836

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown