BEUDAMED
    FDA Adverse Event Injury Summary report: N

    COONRAD/MORREY ULNAR ASSEMBLY

    MDR report key: 1884520 · Received October 19, 2010

    Report

    Report Number
    1822565-2010-00913
    Event Type
    Injury
    Date Received
    October 19, 2010
    Report Date
    May 14, 2010
    Manufacturer
    ZIMMER, INC.
    Product Code
    JDC
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    EVALUATION SUMMARY: NO X-RAYS OR OPERATIVE NOTES WERE RETURNED FOR REVIEW. DUE TO INSUFFICIENT INFO, A ROOT CAUSE OF THE WEAR AND LOOSENING IN THIS CASE CANNOT BE DETERMINED. REVIEW OF THE DEVICE HISTORY RECORDS WAS NOT POSSIBLE AS THE LOT NUMBERS REQUIRED FOR RETRIEVAL WERE UNAVAILABLE. IT IS NOT SUSPECTED THAT THE PRODUCT FAILED TO MEET SPECIFICATIONS. THE INVESTIGATION COULD NOT VERIFY OR IDENTIFY ANY EVIDENCE OF PRODUCT CONTRIBUTION TO THE REPORTED PROBLEM. BASED ON THE AVAILABLE INFO, THE NEED FOR CORRECTIVE ACTION IS NOT INDICATED. SHOULD ADDITIONAL SUBSTANTIVE INFO BE RECEIVED, THE COMPLAINT WILL BE REOPENED. ZIMMER, INC CONSIDERS THE INVESTIGATION CLOSED.

    Description of Event or Problem · 1

    IT IS REPORTED THAT THE PT WAS REVISED FOR BUSHING WEAR AND LOOSENING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 COONRAD/MORREY ULNAR ASSEMBLY ELBOW PROSTHESIS JDC ZIMMER, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 32 YR Required Intervention UNK COONRAD/MORREY ULNAR COMPONENT| CATALOG # UNK, LOT # UNK