BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ON-Q POST-OP PAIN RELIEF SYSTEM

    MDR report key: 790743 · Received December 5, 2006

    Report

    Report Number
    MW1041265
    Event Type
    Injury
    Date Received
    December 5, 2006
    Date of Event
    August 14, 2006
    Report Date
    December 5, 2006
    Manufacturer
    I-FLOW CORP
    Product Code
    MEB
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    ON THE DAY THE PT WAS TO BE DISCHARGED, THE STAFF HAD DIFFICULTY REMOVING A PAIN BALL CATHETER -ON-Q-. AN OB/GYN RESIDENT NEEDED TO PERFORM A MINOR SURGICAL PROCEDURE TO REMOVE IT. AS A RESULT, THE PT'S DISCHARGE WAS DELAYED FOR THREE DAYS.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 30 YR Hospitalization