BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NEGATIVE PRESSURE WOUND THERAPY POWERED SUCTION PUMP

    MDR report key: 4812452 · Received June 2, 2015

    Report

    Report Number
    3006760724-2015-00055
    Event Type
    Injury
    Date Received
    June 2, 2015
    Date of Event
    June 1, 2015
    Report Date
    June 2, 2015
    Manufacturer
    SMITH & NEPHEW, INC.
    Product Code
    OMP
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    HEALTH PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    .

    Description of Event or Problem · 1

    IT WAS REPORTED WHILE USING THE DEVICE, THAT THE PATIENT EXPERIENCED BLEEDING. NO ADDITIONAL INFORMATION IS AVAILABLE AT THIS TIME, HOWEVER REQUESTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    355751 NEGATIVE PRESSURE WOUND THERAPY POWERED SUCTION PUMP NEGATIVE PRESSURE WOUND THERAPY POWERED SUCTION PUMP OMP SMITH & NEPHEW, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1