BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LOVENOX 120MG

    MDR report key: 2132709 · Received June 9, 2011

    Report

    Report Number
    MW5021007
    Event Type
    Malfunction
    Date Received
    June 9, 2011
    Date of Event
    June 8, 2011
    Report Date
    June 9, 2011
    Product Code
    FMF
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    GA, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    THE NEEDLE DID NOT RETRACT AS IT SHOULD ON LOVENOX ENOXAPARIN 120 MG PREFILLED SYRINGE AND NURSE ADMINISTERING THE MEDICATION TO THE PT WAS STUCK WITH THE NEEDLE. DATES OF USE: (B)(6) 2011.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LOVENOX 120MG PREFILLED SYRINGE FMF 15A34

    Patients

    Seq Age Sex Outcome Treatment
    1 Other