BEUDAMED
    FDA Adverse Event Injury Summary report: N

    OXF ANAT BRG LT SM SIZE 4 PMA

    MDR report key: 25091781 · Received May 6, 2026

    Report

    Report Number
    3002806535-2026-00182
    Event Type
    Injury
    Date Received
    May 6, 2026
    Date of Event
    April 13, 2026
    Report Date
    May 6, 2026
    Manufacturer
    BIOMET UK LTD.
    Product Code
    NRA
    UDI-DI
    05019279785872
    PMA / PMN Number
    P010014
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    (B)(4). D10: ITEM NAME#: OXF UNI CMNTLS TIB SZ B LM; ITEM NUMBER#: 166572; LOT NUMBER#: 67091516. ITEM NAME#: OXF TWIN PEG CMNTLS FMRL SM; ITEM NUMBER#: 161473; LOT NUMBER#: 67115595. 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 FOLLOWING A PERIPROSTHETIC FRACTURE OF THE TIBIA, DURING WHICH ALL PROSTHETIC COMPONENTS WERE REMOVED. APPROXIMATELY 25 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
    308957 OXF ANAT BRG LT SM SIZE 4 PMA PROSTHESIS, KNEE, FEMOROTIBIAL, UNICOMPARTMENTAL, SEMI-CONSTRAINED,METAL/POLYMER NRA BIOMET UK LTD. 67501138 05019279785872

    Patients

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