BEUDAMED
    FDA Adverse Event Injury Summary report: N

    FCI RITLENG HOOK

    MDR report key: 18704442 · Received February 13, 2024

    Report

    Report Number
    MW5151582
    Event Type
    Injury
    Date Received
    February 13, 2024
    Date of Event
    January 29, 2024
    Report Date
    February 8, 2024
    Manufacturer
    FCI SAS
    Product Code
    HNQ
    Report Source
    Voluntary report
    Reporter Occupation
    RISK MANAGER
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    TIP OF RITLENG HOOK BROKE OFF DURING PROCEDURE. PATIENT HAD TO HAVE FOLLOW UP X-RAYS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2158816 FCI RITLENG HOOK HOOK, OPHTHALMIC HNQ FCI SAS

    Patients

    Seq Age Sex Outcome Treatment
    1 24 MO Male Required Intervention