BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BARD FLAT MESH

    MDR report key: 3231871 · Received July 10, 2013

    Report

    Report Number
    1213643-2013-00296
    Event Type
    Injury
    Date Received
    July 10, 2013
    Report Date
    June 27, 2013
    Manufacturer
    DAVOL INC., SUB. C.R. BARD, INC.
    Product Code
    FTL
    PMA / PMN Number
    PREAMENDMENT
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    CURRENTLY, IT IS UNK WHETHER THE DEVICE MAY HAVE CAUSED OR CONTRIBUTED TO THE REPORTED EVENT. THE PT'S ATTORNEY DID NOT ALLEGE A SPECIFIC DEVICE FAILURE AND MEDICAL RECORDS HAVE NOT BEEN PROVIDED. WE HAVE CONTACTED THE INITIAL REPORTER TO REQUEST ADDITIONAL INFORMATION AND IF AVAILABLE, TO REQUEST RETURN OF THE DEVICE FOR EVAL. A MANUFACTURING REVIEW WAS PERFORMED AND FOUND NO EVIDENCE OF A MANUFACTURING RELATED CAUSE FOR THE ALLEGED EVENT. THIS MDR INCLUDES ALL PT, EVENT AND DEVICE INFORMATION DAVOL HAS RECEIVED TO DATE. IF ADDITIONAL EVENT AND/OR EVAL INFORMATION IS OBTAINED, A FOLLOW-UP MDR WILL BE SUBMITTED.

    Description of Event or Problem · 1

    THE FOLLOWING WAS REPORTED TO DAVOL BY THE PT'S ATTORNEY: (B)(6) 2006 - THE PT WAS IMPLANTED WITH MULTIPLE MEDICAL DEVICES, INCLUDING A DAVOL FLAT MESH, DURING AN INGUINAL HERNIA REPAIR WITH BLADDER SUSPENSION. THE ATTORNEY'S REPORT ALLEGES ADDITIONAL MEDICAL/SURGICAL TREATMENT, NERVE DAMAGE, PERMANENT INJURY, DEFECTIVE MESH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    318429 BARD FLAT MESH FTL DAVOL INC., SUB. C.R. BARD, INC. NA 43KPD168

    Patients

    Seq Age Sex Outcome Treatment
    1 Disability