BEUDAMED
    FDA Adverse Event Other Summary report: N

    21G ECLIPSE NEEDLE

    MDR report key: 1221811 · Received November 4, 2008

    Report

    Report Number
    1024879-2008-00012
    Event Type
    Other
    Date Received
    November 4, 2008
    Date of Event
    September 10, 2008
    Report Date
    November 4, 2008
    Manufacturer
    BD
    Product Code
    FMI
    PMA / PMN Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MD, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    UPON FURTHER FOLLOW UP WITH THIS ACCOUNT ON 10/27/2008, IT WAS REVEALED THAT THE HCW WHO RECEIVED A NSI WAS PLACED ON PROPHYLACTIC MEDICATION FOR 48 HOURS AND THEN TAKEN OFF.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 21G ECLIPSE NEEDLE 21G ECLIPSE NEEDLE FMI BD NA 7283695

    Patients

    Seq Age Sex Outcome Treatment
    1 NA