BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SCORPIO PS FEMUR WAFFLE POSTS W/LFIT

    MDR report key: 1770231 · Received July 21, 2010

    Report

    Report Number
    2249697-2010-00863
    Event Type
    Injury
    Date Received
    July 21, 2010
    Date of Event
    July 1, 2009
    Report Date
    July 2, 2009
    Manufacturer
    STRYKER ORTHOPAEDICS MAHWAH
    Product Code
    JWH
    PMA / PMN Number
    K962152
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VT, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE FOLLOWING OTHER DEVICES WERE ALSO LISTED IN THIS REPORT: SERIES 7000 STANDARD TIBIA, CAT # 7115-0005; LOT T05L1519. SCORPIO PS TIB INSERT, CAT# 72-3-0508; (B)(4). SCORPIO M-DOME PATELLA, CAT# 73-0510; LOT T406. IT CANNOT BE DETERMINED WHICH, IF ANY OF THESE DEVICES MAY HAVE CAUSED OR CONTRIBUTED TO THE PT'S PAIN. AN EVAL OF THE DEVICE CANNOT BE PERFORMED AS THE DEVICE REMAINED IN THE PT (AS OF (B)(6) 2009) AND WAS NOT RETURNED TO THE MFR. ADDITIONAL INFO WAS REQUESTED. IF DEVICE OR ADDITIONAL INFO BECOMES AVAILABLE, THE EVAL SUMMARY WILL BE SUBMITTED IN A SUPPLEMENTAL REPORT.

    Description of Event or Problem · 1

    IT WAS REPORTED, "THE FOLLOWING INFO WAS OBTAINED VIA A PHONE QUESTIONNAIRE. WHEN THE PT WAS ASKED "DO YOU HAVE ANY PAIN IN YOUR KNEE THAT HAS THE STUDY KNEE REPLACEMENT?" IT WAS NOTED BY THE PERSON CONDUCTING THE PHONE CALL, "MILD, OCCASIONAL WEATHER RELATED SORENESS". THE DATE THE INDIVIDUAL SPOKE TO THE PT VIA PHONE WAS USED AS THE EVENT DATE".

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SCORPIO PS FEMUR WAFFLE POSTS W/LFIT IMPLANT JWH STRYKER ORTHOPAEDICS MAHWAH NA K05L1081

    Patients

    Seq Age Sex Outcome Treatment
    1 73 YR Other