BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LAMINARIA TENT

    MDR report key: 1002025 · Received February 20, 2008

    Report

    Report Number
    MW5005618
    Event Type
    Injury
    Date Received
    February 20, 2008
    Date of Event
    February 18, 2008
    Report Date
    February 20, 2008
    Product Code
    HDY
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    PATIENT ADMITTED TO HOSP. IN PARALYSIS SUSPECTED TO BE CAUSED BY A LAMINARIA TENT. DIAGNOSIS OR REASON FOR USE: ABORTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LAMINARIA TENT HDY

    Patients

    Seq Age Sex Outcome Treatment
    1 YR Hospitalization| S