BEUDAMED
    FDA Adverse Event Injury Summary report: N

    OXF UNI CMNTLS TIB SZ A LM

    MDR report key: 24855644 · Received April 13, 2026

    Report

    Report Number
    3002806535-2026-00149
    Event Type
    Injury
    Date Received
    April 13, 2026
    Date of Event
    March 16, 2026
    Report Date
    April 13, 2026
    Manufacturer
    BIOMET UK LTD.
    Product Code
    NRA
    UDI-DI
    00887868354816
    PMA / PMN Number
    P010014
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    (B)(4). D10: ITEM NAME# OXF ANAT BRG LT SM SIZE 3 PMA; ITEM NUMBER# 159540; LOT NUMBER# 67246097 ITEM NAME# OXF TWIN PEG CMNTLS FMRL SM; ITEM NUMBER# 161473; LOT NUMBER# 67115591 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.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT THE PATIENT UNDERWENT REVISION KNEE SURGERY DUE TO PAIN AND INSTABILITY. ALL EXISTING COMPONENTS WERE REMOVED, AND NEW IMPLANTS WERE SUCCESSFULLY PLACED WITH GOOD FIXATION. APPROXIMATELY 3 MONTHS AND 5 DAYS POST-IMPLANTATION. ATTEMPTS HAVE BEEN MADE, AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    919475 OXF UNI CMNTLS TIB SZ A LM PROSTHESIS, KNEE, FEMOROTIBIAL, UNICOMPARTMENTAL, SEMI-CONSTRAINED,METAL/POLYMER NRA BIOMET UK LTD. 67321855 00887868354816

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Female Hospitalization| R SEE H11 NARRATIVE.