BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TAPERLOC POROUS LATERAL FEMORAL

    MDR report key: 9547041 · Received January 3, 2020

    Report

    Report Number
    0001825034-2020-00023
    Event Type
    Injury
    Date Received
    January 3, 2020
    Date of Event
    December 9, 2019
    Report Date
    April 10, 2020
    Manufacturer
    ZIMMER BIOMET, INC.
    Product Code
    JDI
    PMA / PMN Number
    K830313
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SC, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 0

    (B)(4). UPON RECEIPT OF ADDITIONAL INFORMATION IT HAS BEEN DETERMINED THAT THIS DEVICE DID NOT CAUSE OR CONTRIBUTE TO THE REPORTED EVENT.

    Description of Event or Problem · 0

    UPON RECEIPT OF ADDITIONAL INFORMATION IT HAS BEEN DETERMINED THAT THIS DEVICE DID NOT CAUSE OR CONTRIBUTE TO THE REPORTED EVENT.

    Additional Manufacturer Narrative · 1

    (B)(4). CONCOMITANT MEDICAL PRODUCTS: M2A-MAGNUM PF CUP 54ODX48ID CAT# US157854 LOT# 921250, M2A-MAGNUM MOD HD SZ 48MM CAT# 157448 LOT# 721120, M2A-MAGNUM 42-50MM TPR INSRT-6 CAT# 139252 LOT# 060800. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS; HOWEVER, AN INVESTIGATION OF THE REPORTED EVENT IS IN PROGRESS. ONCE THE INVESTIGATION IS COMPLETED, A SUPPLEMENTAL MEDWATCH 3500A WILL BE SUBMITTED. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034 -2020 -00024, 0001825034 -2020 -00025, 0001825034 -2020 -00026.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL RIGHT HIP ARTHROPLASTY. SUBSEQUENTLY THE PATIENT WAS REVISED APPROXIMATELY 10 YEARS LATER DUE TO PAIN AND ELEVATED METAL ION LEVELS. THE FEMORAL HEAD AND TAPER ADAPTER WERE REMOVED AND REPLACED. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    7792 TAPERLOC POROUS LATERAL FEMORAL PROSTHESIS, HIP JDI ZIMMER BIOMET, INC. NI 188920

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization| R