BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OCTYLSEAL

    MDR report key: 3021395 · Received March 11, 2013

    Report

    Report Number
    3021395
    Event Type
    Malfunction
    Date Received
    March 11, 2013
    Date of Event
    March 7, 2013
    Report Date
    March 11, 2013
    Manufacturer
    CHEMENCE MEDICAL PRODUCTS INC
    Product Code
    MPN
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    CO, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PT ARRIVED IN PACU WITH PART OF THE LINEN SHEET GLUED TO HIS INCISION. IT IS BELIVED THE ADHESIVE HAD NOT DRIED THE ENTIRE AMOUNT BEFORE THE PT WAS TURNED ONTO THE LINEN.WHAT WAS THE ORIGINAL INTENDED PROCEDURE?LUMBAR FUSION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    102678 OCTYLSEAL TISSUE ADHESIVE MPN CHEMENCE MEDICAL PRODUCTS INC * *

    Patients

    Seq Age Sex Outcome Treatment
    1 33 YR