BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TAPERLOC FEMORAL UNCEMENTED STEM

    MDR report key: 2013606 · Received March 10, 2011

    Report

    Report Number
    1825034-2011-00169
    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
    WI, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    THE INFORMATION BEING REPORTED WAS FOUND IN THE JOURNAL ARTICLE TITLED "TOTAL HIP ARTHROPLASTY WITH AN UNCEMENTED TAPERED FEMORAL COMPONENT IN PATIENTS YOUNGER THAN 50 YEARS". JOURNAL ARTHROPLASTY 2010. 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 JR MCLAUGHLIN AND KR LEE. MANUFACTURE DATE - UNKNOWN. THIS REPORT FILED MARCH 10, 2011.

    Description of Event or Problem · 1

    INFORMATION WAS RECEIVED BASED ON REVIEW OF A JOURNAL ARTICLE REFERENCING A RETROSPECTIVE STUDY OF HIP PROCEDURES THAT TOOK PLACE BETWEEN (B)(6) 1983 AND (B)(6) 1990 UTILIZING UNCEMENTED TAPERED FEMORAL COMPONENTS. THE ARTICLE INDICATED THAT ONE REVISION WAS PERFORMED IMMEDIATELY POSTOPERATIVE BECAUSE OF PERONEAL NERVE PALSY SECONDARY TO EXCESSIVE LEG LENGTHENING. THE FEMORAL COMPONENT 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 UNCEMENTED STEM PROSTHESIS, HIP LPH BIOMET ORTHOPEDICS N/A UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization| R