BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    MDR report key: 7573223 · Received June 6, 2018

    Report

    Report Number
    1917413-2018-02140
    Event Type
    Malfunction
    Date Received
    June 6, 2018
    Date of Event
    December 20, 2017
    Report Date
    June 8, 2018
    Manufacturer
    BECTON, DICKINSON & CO.
    Product Code
    JCF
    PMA / PMN Number
    K891407
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    MEDICAL DEVICE TYPE: THIS HAS BEEN CORRECTED TO ¿JCF¿. PMA / 510(K)#:THIS HAS BEEN CORRECTED TO ¿K891407¿.

    Additional Manufacturer Narrative · 1

    DATE OF EVENT: UNKNOWN. THE AWARENESS DATE HAS BEEN USED FOR THIS FIELD. INITIAL REPORTER PHONE#: (B)(6). BD HAD NOT RECEIVED SAMPLES OR PHOTOS FROM THE CUSTOMER FACILITY FOR EVALUATION; THEREFORE, THE INVESTIGATION WAS LIMITED. A REVIEW OF THE MANUFACTURING RECORDS WAS COMPLETED FOR THE INCIDENT LOT AND NO ISSUES WERE IDENTIFIED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT BD VACUTAINER® CPT¿ NH: 130 IU FICOLL¿: 2.0ML TUBES BROKEN IN THE CENTRIFUGE. NO SERIOUS INJURY OR MEDICAL INTERVENTION REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    417614 BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML BLOOD SPECIMEN COLLECTION DEVICE JCF BECTON, DICKINSON & CO. 7251714

    Patients

    Seq Age Sex Outcome Treatment
    1 Other