BEUDAMED
    FDA Adverse Event Summary report: N

    DUOPROSS 3 ML SYRINGE WITH 21G 1" NEEDLE

    MDR report key: 8208532 · Received December 31, 2018

    Report

    Report Number
    MW5082731
    Date Received
    December 31, 2018
    Manufacturer
    DUOPROSS MEDITECH CORPORATION
    Product Code
    FMF
    Report Source
    Voluntary report
    Reporter Occupation
    NO INFORMATION

    Narratives

    Description of Event or Problem · 1

    SYRINGE BARRELS HAVE CRACKS THAT ALLOW LIQUID TO BE RELEASED AS THE PLUNGER IS EXTENDED OR DEPRESSED. (B)(6).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1045062 DUOPROSS 3 ML SYRINGE WITH 21G 1" NEEDLE SYRINGE, PISTON FMF DUOPROSS MEDITECH CORPORATION 20180714

    Patients

    Seq Age Sex Outcome Treatment
    1