BEUDAMED
    FDA Adverse Event Other Summary report: N

    BECTON DICKINSON & COMPANY

    MDR report key: 752429 · Received August 4, 2006

    Report

    Report Number
    MW1039958
    Event Type
    Other
    Date Received
    August 4, 2006
    Date of Event
    July 18, 2006
    Report Date
    August 4, 2006
    Manufacturer
    BECTON DICKINSON & COMPANY
    Product Code
    FMF
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    SC, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    PT BOUGHT BAGS OF SEALED INSULIN SYRINGES RECEIVED THRU THE MAIL THAT APPEARED TO BE CONTAMINATED WITH BLOOD. ASKED PT TO KEEP REMAINING SUPPLY IN A SEALED BAG FOR FURTHER INSPECTION. PT SCREENED FOR HIV, RPR, & HEPATITIS WHICH WERE NEGATIVE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BECTON DICKINSON & COMPANY BD ULTRAFINE II INSULIN SYRINGES FMF BECTON DICKINSON & COMPANY * 328289

    Patients

    Seq Age Sex Outcome Treatment
    1 41 YR Other