BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TAPERLOC FEMORAL STEM

    MDR report key: 2013642 · Received March 10, 2011

    Report

    Report Number
    1825034-2011-00176
    Event Type
    Injury
    Date Received
    March 10, 2011
    Report Date
    February 11, 2011
    Manufacturer
    BIOMET ORTHOPEDICS
    Product Code
    LPH
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    THE INFORMATION BEING REPORTED WAS FOUND IN A JOURNAL ARTICLE TITLED "TOTAL HIP ARTHROPLASTY USING TWO DIFFERENT CEMENTLESS TAPERED STEMS". CLIN ORTHOP REL RES 2001; 393:1212-1217 CURRENT INFORMATION IS INSUFFICIENT TO PERMIT A CONCLUSION AS TO THE CAUSE OF THE EVENT. EVENT DETAILS AND PRODUCT IDENTIFICATION WAS NOT PROVIDED FOR THE REVISION MENTIONED IN THE JOURNAL ARTICLE. DATE OF EVENT - UNKNOWN. EXPIRATION DATE - UNKNOWN. DATE IMPLANTED - UNKNOWN. DATE EXPLANTED - UNKNOWN. INITIAL REPORTER - THE ARTICLE WAS WRITTEN BY RH ROTHMAN, JJ PURTILL, WJ HOZACK AND PF SHARKEY. MANUFACTURE DATE - UNKNOWN (B)(4).

    Description of Event or Problem · 1

    INFORMATION WAS RECEIVED BASED ON A REVIEW OF A JOURNAL ARTICLE REFERENCING A RETROSPECTIVE STUDY OF TOTAL HIP PROCEDURES THAT TOOK PLACE BETWEEN (B)(6) 1986 AND (B)(6) 1987 UTILIZING TAPERLOC FEMORAL STEMS. THE ARTICLE INDICATED THAT A REVISION PROCEDURE WAS PERFORMED DUE TO PROXIMAL FEMORAL OSTEOLYSIS. THE FEMORAL STEM WAS REMOVED AND REPLACED. NO FURTHER INFORMATION HAS BEEN PROVIDED TO DATE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TAPERLOC FEMORAL STEM PROSTHESIS, HIP LPH BIOMET ORTHOPEDICS N/A UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization| R