BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BD POSIFLUSH

    MDR report key: 2072646 · Received April 21, 2011

    Report

    Report Number
    1911916-2011-00005
    Event Type
    Injury
    Date Received
    April 21, 2011
    Report Date
    April 21, 2011
    Manufacturer
    BECTON DICKINSON
    Product Code
    FOZ
    PMA / PMN Number
    K003553
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    A HEALTHCARE WORKER OPENED THE TUB OF 30 SYRINGES AND NOTICED A LIQUID GEL IN THE TUB WITH A VERY STRONG SMELL. OTHER HEALTHCARE WORKERS THEN LOOKED AT THE TUB AND HAD SYMPTOMS OF A BURNING SENSATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BD POSIFLUSH 10ML FILL IN 10ML SALINE FLUSH SYRINGE FOZ BECTON DICKINSON NA 0357296

    Patients

    Seq Age Sex Outcome Treatment
    1 Other