BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PEN NDL 32G 4MM 90 CT MAIL ORDER ONLY

    MDR report key: 19134201 · Received April 18, 2024

    Report

    Report Number
    9616656-2024-05266
    Event Type
    Malfunction
    Date Received
    April 18, 2024
    Date of Event
    March 26, 2024
    Report Date
    April 18, 2024
    Manufacturer
    BECTON DICKNSON AND CO. - DUN LAOGHAIRE CO, IRELAND
    Product Code
    FMI
    PMA / PMN Number
    K213478
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    15-20 PEN NEEDLES AFFECTED BY EVENT. 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. DEVICE IS NOT AVAILABLE.

    Description of Event or Problem · 0

    CONSUMER REPORTED FOUND 15-20 PEN NEEDLES THAT WOULD NOT COMPLETE INJECTION. INFORMED CONSUMER OF PROPER NON PATIENT END PLACEMENT. DC LOT # 3172420. CATALOG# 320883. DATE OF EVENT 03/26/2024. SAMPLE STATUS DISCARD . SENDING REPLACEMENT TO DOCTORS OFFICE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2237761 PEN NDL 32G 4MM 90 CT MAIL ORDER ONLY Needle, hypodermic, single lumen FMI BECTON DICKNSON AND CO. - DUN LAOGHAIRE CO, IRELAND 320883 3172420

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown