BEUDAMED
    FDA Adverse Event Other Summary report: N

    BD

    MDR report key: 303839 · Received November 7, 2000

    Report

    Report Number
    MW1020355
    Event Type
    Other
    Date Received
    November 7, 2000
    Date of Event
    November 6, 2000
    Report Date
    November 7, 2000
    Manufacturer
    BD & CO.
    Product Code
    FME
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    UNKNOWN MATERIAL ON HUB OF NEEDLE BASE. POSSIBLE BANDING SOLVENT FROM MFG.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BD 3ML 22GX1 SYRINGE & NEEDLE FME BD & CO. * 0E118

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other