BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PEN NDL 32G 4MM PRO 100 BOX 1200 CA

    MDR report key: 19153735 · Received April 22, 2024

    Report

    Report Number
    3023359743-2024-00010
    Event Type
    Malfunction
    Date Received
    April 22, 2024
    Report Date
    April 22, 2024
    Manufacturer
    EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND
    Product Code
    FMI
    PMA / PMN Number
    UNKNOWN
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    INVESTIGATION SUMMARY: NO SAMPLES (INCLUDING PHOTOS) WERE RETURNED THEREFORE THE COMPLAINT COULD NOT BE CONFIRMED AND THE ROOT CAUSE IS UNDETERMINED. THIS IS THE 1ST COMPLAINT FOR THE REPORTED LOT NUMBER. A REVIEW OF THE MANUFACTURING RECORDS WAS PERFORMED, AND NO NON-CONFORMANCES WERE RAISED IN ASSOCIATION WITH THIS TYPE OF EVENT FOR THIS LOT. COMPLAINTS RECEIVED FOR THIS DEVICE AND REPORTED CONDITION WILL CONTINUE TO BE TRACKED AND TRENDED. IF SAMPLES ARE RECEIVED IN THE FUTURE THE COMPLAINT WILL BE REOPENED FOR FURTHER INVESTIGATION. BASED ON THE ABOVE, NO ADDITIONAL INVESTIGATION AND NO CORRECTIVE/PREVENTATIVE ACTION (CAPA) OR SITUATIONAL ANALYSIS (SA) IS REQUIRED AT THIS TIME. H3 OTHER TEXT : DEVICE IS NOT AVAILABLE.

    Description of Event or Problem · 0

    SPOUSE OF CONSUMER STATED, NO INSULIN FLOW WHEN TAKING INJECTION. WHEN ASKED IF THE PEN NEEDLE WAS PRIMED BEFORE TAKING INJECTION, THE WIFE STATED, "SOME DROP COME OUT" STATED, SHE DOES NOT FOLLOW THE INSTRUCTIONS ON THE BOX. LOT: 3172409 CATALOG: 320555 DATE OF EVENT: UNKNOWN SAMPLES: NO CL

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2589063 PEN NDL 32G 4MM PRO 100 BOX 1200 CA Needle, hypodermic, single lumen FMI EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND 320555 3172409

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown