BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MONOJECT SYRINGE WITH LUER LOCK

    MDR report key: 33681 · Received June 21, 1996

    Report

    Report Number
    MW1009354
    Event Type
    Malfunction
    Date Received
    June 21, 1996
    Manufacturer
    SHERWOOD MEDICAL CO.
    Product Code
    FMF
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MI, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    THE 20CC LUER LOCK SYRINGE IS RESISTANT TO INFUSION BY ANOTHER MFR'S PUMP WHEN GREATER THAN 10CC IS USED IN SYRINGE. PLUNGER IS STICKING AND MUST BE MANUALLY INFUSED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MONOJECT SYRINGE WITH LUER LOCK SYRINGE FMF SHERWOOD MEDICAL CO. 727070

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO