BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNKNOWN PERMACOL PRODUCT

    MDR report key: 5251406 · Received November 25, 2015

    Report

    Report Number
    9617613-2015-00024
    Event Type
    Injury
    Date Received
    November 25, 2015
    Report Date
    November 25, 2015
    Manufacturer
    COVIDIEN, FORMERLY TISSUE SCIENCE LABOR
    Product Code
    FTM
    PMA / PMN Number
    K120605
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AU
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4).

    Additional Manufacturer Narrative · 1

    (B)(4). AS NO LOT NUMBER WAS PROVIDED, A REVIEW OF THE DEVICE HISTORY RECORD COULD NOT BE PERFORMED. ALL PROCESS AND TEST CRITERIA ARE VERIFIED AS COMPLYING WITH THE FINISHED PRODUCT SPECIFICATIONS FOR ALL RELEASED LOTS. A REVIEW OF HISTORICAL COMPLAINT DATA DISPLAYED NO INCREASE IN TRENDS. SHOULD ADDITIONAL INFORMATION BE RECEIVED, THE RECORD WILL BE REASSESSED AT THAT TIME. LITERATURE REFERENCE: HTTP://WWW.RESEARCHGATE.NET/PROFILE/HEINZ_BACHER/PUBLICATION/266322811_EFFECTIVENESS_OF_PORCINE_DERMAL_COLLAGEN_IN_GIANT_HERNIA_CLOSURE_IN_PATIENTS_WITH_DELETERIOUS_FASCIA_CONSTITUTION_AFTER_ORTHOTOPIC_LIVER_TRANSPLANTATION/LINKS/5444C32F0CF2A76A3CCD8488.PDF.

    Description of Event or Problem · 1

    ADDITIONAL INFORMATION RECEIVED FROM THE REPORTER INDICATED THAT, IN HER MEDICAL OPINION, THE COMPLICATION RESULTING FROM THE SURGICAL REPAIR AND IMPLANT WAS A RESULT OF THE PATIENT'S GENERAL CONDITION THAT WAS MARKED BY IMMUNOSUPPRESIVE REGIMEN, DIABETES AND CONSISTENCY OF THE ABDOMINAL WALL ITSELF. THERE WAS NO ALLEGED RELATIONSHIP BETWEEN THE DEVICE AND THE PATIENT ADVERSE EVENT.

    Description of Event or Problem · 1

    ACCORDING TO THE REPORTER, THE AIM OF THIS STUDY WAS TO EVALUATE THE EFFECTIVENESS OF PORCINE DERMAL COLLAGEN (PDC) FOR THE CLOSURE OF INCISIONAL HERNIAS (IH) AFTER ORTHOTOPIC LIVER TRANSPLANTATION (OLT). PATIENTS WITH A PRIMARY IH GREATER THAN 10CM IN DIAMETER AFTER OLT WERE INCLUDED. 16 PATIENTS RECEIVED THE PDC MESH; AFTER A PREOPERATIVE SINGLE INJECTION OF 1.5G CEFUROXIME AS ANTIBIOTIC PROPHYLAXIS, THE HERNIA REPAIR WAS PERFORMED WITH A CROSS LINKED PDC MESH PLACEMENT USING BRIDGING TECHNIQUE. THE MESH WAS FIXED USING INTERRUPTED STITCHES WITH MONOFIL FILAMENT. A 14 FRENCH REDON DRAINAGE WAS PLACED ON TOP OF THE MESH. ALL PATIENTS RECEIVED SUBCUTANEOUS INTERRUPTED SUTURES WITH VICRYL 2/0 SUTURES. THE SKIN WAS SUTURED INTRACUTANEOUSLY, AND STERILE DRESSINGS WERE APPLIED." THE IMMUNOSUPPRESSIVE REGIMEN CONSISTED OF MYCOPHENOLATE MOFETIL (1000MG BID FOR ALL PATIENTS) IN COMBINATION WITH TACROLIMUS (9/16 PATIENTS) OR MTOR (MAMMALIAN TARGET OF RAPAMYCIN) INHIBITORS (7/16 PATIENTS); 1 OF THE 16 PATIENTS RECEIVED 5MG OF PREDNISOLONE DAILY. POSTOPERATIVE INFECTION ABOVE THE MESH OCCURRED IN FOUR PATIENTS. THE INFECTION WAS MANAGED WITH ADMINISTRATION OF ANTIBIOTICS AND SURGICAL DRAINAGE. ADDITIONAL INFORMATION HAS BEEN REQUESTED BUT NOT YET RECEIVED. A SUPPLEMENTAL WILL BE SUBMITTED SHOULD THE INFORMATION BE MADE AVAILABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    779672 UNKNOWN PERMACOL PRODUCT MESH, SURGICAL FTM COVIDIEN, FORMERLY TISSUE SCIENCE LABOR

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention