BEUDAMED
    FDA Adverse Event Death Summary report: N

    PALACOS BONE CEMENT

    MDR report key: 472999 · Received July 18, 2003

    Report

    Report Number
    1825034-2003-00077
    Event Type
    Death
    Date Received
    July 18, 2003
    Date of Event
    August 20, 2001
    Report Date
    June 27, 2003
    Manufacturer
    BIOMET, INC.
    Product Code
    LOD
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AL, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Description of Event or Problem · 1

    PT ALLEGEDLY UNDERWENT CEMENTED TOTAL HIP ARTHROPLASTY. PT EXPIRED 2 DAYS LATER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PALACOS BONE CEMENT BONE CEMENT LOD BIOMET, INC. NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Death