BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ON Q PAIN BUSTER-POST OP PAIN RELIEF SYSTEM

    MDR report key: 1180451 · Received September 29, 2008

    Report

    Report Number
    MW5008477
    Event Type
    Injury
    Date Received
    September 29, 2008
    Date of Event
    September 27, 2008
    Report Date
    September 29, 2008
    Manufacturer
    I-FLOW CORPORATION
    Product Code
    MEB
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NV, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    ON Q PUMP CATHETER WAS REMOVED IN 2008 AND A PORTION OF THE CATHETER WAS LEFT INSIDE THE OPERATIVE AREA. THE PT HAD TO RETURN TO OR IN THE NEXT DAY FOR THE REMOVAL OF THE RETAINED PORTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ON Q PAIN BUSTER-POST OP PAIN RELIEF SYSTEM ON Q MEB I-FLOW CORPORATION

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization| R