BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACETABULAR REAMER HANDLE

    MDR report key: 2053627 · Received March 17, 2011

    Report

    Report Number
    2249697-2011-00324
    Event Type
    Malfunction
    Date Received
    March 17, 2011
    Date of Event
    February 21, 2011
    Report Date
    February 23, 2011
    Manufacturer
    STRYKER ORTHOPAEDICS MAHWAH
    Product Code
    LXH
    PMA / PMN Number
    NA
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A SUPPLEMENTAL REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT, "HANDLE BROKE WHILE REAMING."

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACETABULAR REAMER HANDLE INSTRUMENT LXH STRYKER ORTHOPAEDICS MAHWAH NA V51611

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Required Intervention