BEUDAMED
    FDA Adverse Event Other Summary report: N

    BD BACTECT BLOOD CULTURE PROCEDURAL TRAY 1

    MDR report key: 618579 · Received August 5, 2004

    Report

    Report Number
    1119779-2004-00004
    Event Type
    Other
    Date Received
    August 5, 2004
    Date of Event
    July 15, 2004
    Report Date
    August 2, 2004
    Manufacturer
    BD DIAGNOSTICS
    Product Code
    MDB
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KS, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    PATIENT HAD A BLOOD CULTURE COLLECTED USING THE BD BACTECT BLOOD CULTURE PROCEDURAL TRAY 1. SUBSEQUENT TO THE BLOOD COLLECTION, THE PATIENT EXPERIENCED AN ALLERGIC REACTION THAT REQUIRED MEDICAL INTERVENTION, ADMINISTRATION OF STEROIDS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BD BACTECT BLOOD CULTURE PROCEDURAL TRAY 1 BLOOD CULTURE COLLECTION KIT MDB BD DIAGNOSTICS NA 4091669

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other| R