BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PROG VALVE CLYNDRICAL

    MDR report key: 16684206 · Received April 5, 2023

    Report

    Report Number
    3013886523-2023-00098
    Event Type
    Injury
    Date Received
    April 5, 2023
    Date of Event
    February 21, 2023
    Report Date
    June 3, 2023
    Manufacturer
    INTEGRA LIFESCIENCES MANSFIELD
    Product Code
    JXG
    UDI-DI
    10381780519188
    PMA / PMN Number
    K122118
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER
    Health Professional
    N

    Narratives

    Additional Manufacturer Narrative · 0

    DHR - LOT 5871131,CONFORMED TO THE SPECIFICATIONS WHEN RELEASED TO STOCK. FAILURE ANALYSIS - THE VALVE WAS VISUALLY INSPECTED: NO DEFECTS NOTED. THE VALVE PASSED THE TESTS FOR PROGRAMMING, OCCLUSION, LEAKS, REFLUX AND PRESSURE. ROOT CAUSE - NO ROOT CAUSE COULD BE DETERMINED FOR THE ISSUE REPORTED BY THE CUSTOMER AS THE TECHNICIAN COULD NOT CONFIRM ANY PROBLEMS WITH THE VALVE AT THE TIME OF INVESTIGATION. THE POSSIBLE ROOT CAUSE FOR THE ISSUE REPORTED BY THE CUSTOMER, COULD BE DUE TO BIOLOGICAL DEBRIS AND PROTEIN BUILD UP INTERFERING WITH THE VALVE MECHANISM, AT THE TIME OF INVESTIGATION NO OCCLUSION ISSUES WERE NOTED.

    Additional Manufacturer Narrative · 0

    AN INVESTIGATION HAS BEEN INITIATED BASED ON THE REPORTED INFORMATION. UPON COMPLETION OF THE INVESTIGATION, A FOLLOW-UP REPORT WILL BE SUBMITTED.

    Description of Event or Problem · 0

    N/A.

    Description of Event or Problem · 0

    A FACILITY REPORTED A HAKIM VALVE (ID 823115) WAS BLOCKED AND MEDICAL STAFF HAD TO EXPLANT IT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2254691 PROG VALVE CLYNDRICAL CHPV JXG INTEGRA LIFESCIENCES MANSFIELD 823115 5871131 10381780519188

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown