BEUDAMED
    FDA Adverse Event Injury Summary report: N

    VANG XP INLK FEMORAL L52.5

    MDR report key: 7310175 · Received March 2, 2018

    Report

    Report Number
    0001825034-2018-01313
    Event Type
    Injury
    Date Received
    March 2, 2018
    Date of Event
    August 23, 2016
    Report Date
    February 22, 2018
    Manufacturer
    ZIMMER BIOMET, INC.
    Product Code
    MBH
    Removal / Correction Number
    N/A
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    JA
    Reporter Occupation
    HEALTH PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034-2018-01314, 0001825034-2018-01315, 0001825034-2018-01316. CONCOMITANT PRODUCTS: CAT 195751 ¿ LOT 585400 ¿ VANG XP INLK PRI TIB TRAY; CAT 195807 ¿ LOT 173550 - VGXP XP LAT TIB BRG LT; CAT 195878 ¿ LOT 979020 - VGXP XP MED TIB BRG LT. REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. THE PRODUCT WAS NOT RETURNED FOR THE INVESTIGATION, THEREFORE A VISUAL AND DIMENSIONAL EVALUATIONS COULD NOT BE PERFORMED. DHR WAS REVIEWED AND NO DISCREPANCIES WERE FOUND. ROOT CAUSE WAS UNABLE TO BE DETERMINED AS THE NECESSARY INFORMATION TO ADEQUATELY INVESTIGATE THE REPORT EVENT WAS NOT REPORTED. 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. THIS REPORT IS BEING SUBMITTED LATE AS IT HAS BEEN IDENTIFIED IN REMEDIATION.

    Description of Event or Problem · 1

    IT WAS REPORTHED THAT THE PATIENT HAD KNEE IMPLANTATION IN BOTH THE KNEES. POST-OPERATIVELY, THE PATIENT HAS MENTIONED PROBLEMS WITH LEFT KNEE THAT INCLUDE MODERATE PAIN STANDING UP, OCCASIONAL LIMPING, IMPOSSIBLE TO KNEEL, INTERFERENCE WITH WORK DUE TO PAIN AND MODERATE DIFFICULTY IN WALKING DOWN STAIRS DURING THE SIX MONTH FOLLOW UP VISIT. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    153497 VANG XP INLK FEMORAL L52.5 PROSTHESIS, KNEE MBH ZIMMER BIOMET, INC. NI 331390

    Patients

    Seq Age Sex Outcome Treatment
    1 74 YR Other