BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RESTORE 5X10 SELF-TAPPING IMPLANT WITH MOUNT

    MDR report key: 186265 · Received September 10, 1998

    Report

    Report Number
    2184002-1998-00599
    Event Type
    Injury
    Date Received
    September 10, 1998
    Date of Event
    July 9, 1998
    Report Date
    September 10, 1998
    Manufacturer
    LIFECORE BIOMEDICAL, INC.
    Product Code
    DZE
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    IMPLANT WAS PLACED 04/07/1998. IT WAS LOOSE WHEN UNCOVERED AND REMOVED 07/09/1998.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RESTORE 5X10 SELF-TAPPING IMPLANT WITH MOUNT Implant ENDOSSEOUS IMPLANT DZE LIFECORE BIOMEDICAL, INC. R9010-50-10 75980813

    Patients

    Seq Age Sex Outcome Treatment
    1 31 YR Required Intervention