BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BIOMET CC I-BEAM TRAY 71MM

    MDR report key: 7760049 · Received August 7, 2018

    Report

    Report Number
    0001825034-2018-06604
    Event Type
    Injury
    Date Received
    August 7, 2018
    Date of Event
    April 13, 2006
    Report Date
    September 24, 2018
    Manufacturer
    ZIMMER BIOMET, INC.
    Product Code
    JWH
    PMA / PMN Number
    PK142933
    Removal / Correction Number
    N/A
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). CONCOMITANT MEDICAL PRODUCTS: ITEM # 183010, VANGUARD CR ILOK FEM-LT 65, LOT # UNKNOWN; ITEM # UNKNOWN, BIOMET ARCOS PATELLA, LOT # UNKNOWN; ITEM # 183440, VNGD CR TIB BRG 10X71/75, LOT # UNKNOWN. CUSTOMER HAS INDICATED THAT THE PRODUCT WILL NOT BE RETURNED BECAUSE IT REMAINS IMPLANTED. THE INVESTIGATION IS IN PROCESS. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED. MULTIPLE MDR REPORTS WERE FILLED FOR THIS EVENT: 0001825034-2018-06601, 0001825034-2018-06603 AND 0001825034-2018-06602.

    Additional Manufacturer Narrative · 1

    THIS FOLLOW-UP REPORT IS BEING SUBMITTED TO RELAY ADDITIONAL INFORMATION. REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. DEVICE HISTORY RECORD (DHR) REVIEW WAS UNABLE TO BE PERFORMED AS THE LOT NUMBER OF THE DEVICE INVOLVED IN THE EVENT IS UNKNOWN. ROOT CAUSE WAS UNABLE TO BE DETERMINED. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS.

    Description of Event or Problem · 1

    IT WAS REPORTED A PATIENT UNDERWENT RIGHT PRIMARY TOTAL KNEE ARTHROPLASTY. PATIENT WAS NOTED TO HAVE A URINARY TRACK INFECTION TWICE POSTOPERATIVELY. PATIENT WAS TREATED WITH LEVAQUIN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    596925 BIOMET CC I-BEAM TRAY 71MM PROSTHEISIS KNEE JWH ZIMMER BIOMET, INC. N/A UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 56 YR Required Intervention