BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SULZER SPINE-TECH BONE HARVESTER

    MDR report key: 234204 · Received July 30, 1999

    Report

    Report Number
    2184052-1999-00006
    Event Type
    Injury
    Date Received
    July 30, 1999
    Date of Event
    May 5, 1999
    Report Date
    July 30, 1999
    Manufacturer
    SULZER SPINE-TECH
    Product Code
    HRX
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    THE CUTTING HEAD OF THE POWER BONE HARVESTER BROKE OFF OF THE INSTRUMENT DURING USE AND COULD NOT BE RETRIEVED FROM THE ILIAC CREST.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SULZER SPINE-TECH BONE HARVESTER AUTOGENOUS BONE HARVESTER HRX SULZER SPINE-TECH NA P980562

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other