BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNKNOWN KNEE

    MDR report key: 7114450 · Received December 13, 2017

    Report

    Report Number
    0001825034-2017-11139
    Event Type
    Injury
    Date Received
    December 13, 2017
    Report Date
    December 13, 2017
    Manufacturer
    ZIMMER BIOMET, INC.
    Product Code
    JWH
    PMA / PMN Number
    PN/A
    Removal / Correction Number
    N/A
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). REPORTED EVENT WAS UNABLE TO BE CONFIRMED AS PART NUMBER AND LOT NUMBER OF THE DEVICE INVOLVED IN THE INCIDENT IS UNKNOWN. DEVICE HISTORY RECORD REVIEW WAS UNABLE TO BE PERFORMED AS THE LOT NUMBER OF THE DEVICE INVOLVED IN THE EVENT IS UNKNOWN. ROOT CAUSE WAS UNABLE TO BE DETERMINED AS THE NECESSARY INFORMATION TO ADEQUATELY INVESTIGATE THE REPORTED EVENT WAS NOT PROVIDED. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS. RITTER, MERRILL A. . ¿FLAT-ON-FLAT, NONCONSTRAINED, COMPRESSION MOLDED POLYETHYLENE TOTAL KNEE REPLACEMENT.¿ CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, VOL. 321, 1995, PP. 79¿85.

    Description of Event or Problem · 1

    REVISION DUE TO UNKNOWN FAILURES

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    895210 UNKNOWN KNEE KNEE PROSTHESIS JWH ZIMMER BIOMET, INC. NI UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1