BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNKNOWN ZIMMER STEM

    MDR report key: 5149702 · Received October 14, 2015

    Report

    Report Number
    1822565-2015-02150
    Event Type
    Injury
    Date Received
    October 14, 2015
    Report Date
    September 18, 2015
    Manufacturer
    ZIMMER INC
    Product Code
    KWZ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    NO DEVICE WAS RECEIVED AS IT REMAINED IMPLANTED; THEREFORE THE CONDITION OF THE DEVICE IS UNKNOWN. THE PART AND LOT NUMBERS OF THE PRODUCT IS UNKNOWN; THEREFORE THE DEVICE HISTORY RECORDS, COMPLAINT HISTORY COULD NOT BE REVIEWED. THE REPORTED DEVICE IS USED FOR TREATMENT. IT COULD NOT BE CONFIRMED IF THE DEVICE WAS USED IN AN APPROVED AND COMPATIBLE COMBINATION. SURGICAL NOTES WERE NOT PROVIDED. RELEVANT MEDICAL HISTORY IS UNKNOWN. A DEFINITIVE ROOT CAUSE CANNOT BE DETERMINED WITH THE INFORMATION PROVIDED.

    Additional Manufacturer Narrative · 1

    INFORMATION WAS RECEIVED VIA PUBLISHED LITERATURE. PLEASE REFERENCE LITERATURE AT THE FOLLOWING LOCATION: HTTP://LINK.SPRINGER.COM/ARTICLE/10.1007%2FS11999-013-3167-4/FULLTEXT.HTML. (B)(4). THIS REPORT WILL BE AMENDED WHEN OUR INVESTIGATION IS COMPLETE.

    Description of Event or Problem · 1

    IT IS REPORTED THAT ONE INTRAOPERATIVE PROXIMAL FEMORAL SHAFT FRACTURE WAS TREATED WITH CERCLAGE CABLES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    679624 UNKNOWN ZIMMER STEM HIP PROSTHESIS KWZ ZIMMER INC

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention