BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SYRINGE 0.3ML 30GA 8MM 10BAG 500 L AMR

    MDR report key: 19806269 · Received July 23, 2024

    Report

    Report Number
    3024508819-2024-00208
    Event Type
    Malfunction
    Date Received
    July 23, 2024
    Date of Event
    June 28, 2024
    Report Date
    October 16, 2024
    Manufacturer
    EMBECTA MEDICAL I LLC - HOLDREGE, NE
    Product Code
    FMF
    PMA / PMN Number
    UNKNOWN
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    OTHER
    Health Professional
    N

    Narratives

    Additional Manufacturer Narrative · 0

    INVESTIGATION SUMMARY: NO PHYSICAL SAMPLES WERE RECEIVED HOWEVER THE INVESTIGATION WAS PERFORMED BASED ON THE PHOTO(S) PROVIDED. 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. EMBECTA WAS ABLE TO DUPLICATE OR CONFIRM THE INDICATED ISSUE AND BASED ON TREND ANALYSIS NO FURTHER ACTION IS REQUIRED AT THIS TIME. 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 SITUATION ANALYSIS (SA) IS REQUIRED AT THIS TIME.

    Description of Event or Problem · 0

    EAN PRINTED INCORRECTLY. THE BARCODE NUMBERS CANNOT BE SEEN. MATERIAL: AG BD ULTRA FINE II 8MM 30UN MINI MATERIAL #: 328322 LOT: 1123322 B THE IMAGE IN ANNEX IS IN PHOTO #4.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1046378 SYRINGE 0.3ML 30GA 8MM 10BAG 500 L AMR SYRINGE, PISTON FMF EMBECTA MEDICAL I LLC - HOLDREGE, NE 328322 1123322

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Female