BEUDAMED
    FDA Adverse Event Other Summary report: N

    MONOJECT CURVED TIP SYRINGE

    MDR report key: 261445 · Received February 2, 2000

    Report

    Report Number
    1915484-2000-00002
    Event Type
    Other
    Date Received
    February 2, 2000
    Date of Event
    January 4, 2000
    Report Date
    February 1, 2000
    Manufacturer
    THE KENDALL COMPANY
    Product Code
    ECB
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    DENTAL HYGIENIST

    Narratives

    Description of Event or Problem · 1

    CUSTOMER PHONED IN COMPLAINT TO MFR ON 01/04/2000, STATING BEING STUCK BY A NEEDLE THAT WAS FOUND IN A BOX OF CURVED TIP DENTAL SYRINGES. THE BOX OF SYRINGES PT WAS PLACING HAND INTO HAD NO ATTACHED NEEDLE, HOWEVER, CUSTOMER ADMITS BEING STUCK BY A 5CC SYRINGE WITH AN ATTACHED NEEDLE. CUSTOMER REPORTS THAT NEEDLE WAS A BD PLASTIC PACK, AND THE WORDS DISCARD IT WERE WRITTEN ON THE SYRINGE BARREL. CUSTOMER REPORTS THAT NEEDLE PENETRATED THE SKIN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MONOJECT CURVED TIP SYRINGE DENTAL SYRINGE ECB THE KENDALL COMPANY * NO1364

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other